The currently used anthelmintic drugs, in single oral application, have low efficacy against Trichuris trichiura infection, and hence novel anthelmintic drugs are needed. Nitazoxanide has been suggested as potential drug candidate.
The efficacy and safety of a single oral dose of nitazoxanide (1,000 mg), or albendazole (400 mg), and a nitazoxanide-albendazole combination (1,000 mg–400 mg), with each drug administered separately on two consecutive days, were assessed in a double-blind, randomized, placebo-controlled trial in two schools on Pemba, Tanzania. Cure and egg reduction rates were calculated by per-protocol analysis and by available case analysis. Adverse events were assessed and graded before treatment and four times after treatment.
Complete data for the per-protocol analysis were available from 533 T. trichiura-positive children. Cure rates against T. trichiura were low regardless of the treatment (nitazoxanide-albendazole, 16.0%; albendazole, 14.5%; and nitazoxanide, 6.6%). Egg reduction rates were 54.9% for the nitazoxanide-albendazole combination, 45.6% for single albendazole, and 13.4% for single nitazoxanide. Similar cure and egg reduction rates were calculated using the available case analysis. Children receiving nitazoxanide had significantly more adverse events compared to placebo recipients. Most of the adverse events were mild and had resolved within 24 hours posttreatment.
Nitazoxanide shows no effect on T. trichiura infection. The low efficacy of albendazole against T. trichiura in the current setting characterized by high anthelmintic drug pressure is confirmed. There is a pressing need to develop new anthelmintics against trichuriasis.
More than 5 billion people are at risk of infection with one of the three most common intestinal worms, the roundworm Ascaris lumbricoides, the whipworm Trichuris trichiura, and two different kinds of hookworms. The global strategy to control these intestinal worm infections is through the regular administration of deworming drugs to school-aged children (albendazole, 400 mg; mebendazole, 500 mg). However, especially against T. trichiura, a low treatment response is observed with single doses of both drugs. We tested the antiprotozoal drug nitazoxanide, which had shown promising trichuricidal properties in in vitro experiments. A randomized controlled trial was carried out on the island of Pemba in Tanzania. Four treatment arms were included: (i) single albendazole (400 mg), (ii) single nitazoxanide (1,000 mg), (iii) nitazoxanide-albendazole combination (1,000 mg–400 mg) with each drug given separately on two consecutive days, and (iv) placebo. Children were asked for adverse events at several time points after treatment. Nitazoxanide showed no ability to cure T. trichiura-infected children and caused significantly more mild adverse events than placebo. Albendazole and the nitazoxanide-albendazole combination showed only a minimal effect against T. trichiura. Our results emphasize the urgent need to develop new, safe, and effective anthelmintic drugs against T. trichiura.
Citation: Speich B, Ame SM, Ali SM, Alles R, Hattendorf J, Utzinger J, et al. (2012) Efficacy and Safety of Nitazoxanide, Albendazole, and Nitazoxanide-Albendazole against Trichuris trichiura Infection: A Randomized Controlled Trial. PLoS Negl Trop Dis 6(6): e1685. doi:10.1371/journal.pntd.0001685
Editor: Michael Cappello, Yale Child Health Research Center, United States of America
Received: March 23, 2012; Accepted: April 27, 2012; Published: June 5, 2012
Copyright: © 2012 Speich et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This trial was financially supported by the Vontobel Foundation and the University of Basel. JK is grateful to the Swiss National Science Foundation (projects no. PPOOA-114941 and PPOOP3_135170) for a personal career development grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Infections with the soil-transmitted helminths, Ascaris lumbricoides, Trichuris trichiura, and the two hookworm species Ancylostoma duodenale and Necator americanus, are the most common infections of humans, causing an estimated global burden of 39 million disability-adjusted life years lost (DALYs) –. Globally more than 5 billion people are at risk and at least 1 billion people are currently infected with one or several of these nematodes , , . On Pemba, soil-transmitted helminth infections remain of considerable public health importance with particularly high prevalences observed for T. trichiura and hookworm .
Preventive chemotherapy targeting at-risk communities (i.e., school-aged children) is in place in many countries. These programs aim at morbidity control, and hence intensity of infection is kept below a threshold of disease . The two benzimidazoles, albendazole and mebendazole, as well as pyrantel pamoate and levamisole are recommended drugs against infections with soil-transmitted helminths , . These drugs have been widely used as they were developed and put on the market between 1966 (pyrantel pamoate) and 1980 (albendazole) . The four drugs exhibit distinct differences in their therapeutic profile, with the exception of considerably high efficacy of all drugs against A. lumbricoides. For the treatment of hookworm infection, only albendazole achieves satisfactory cure rates when administered as a single oral dose. Of particular concern is the situation for T. trichiura; single doses of mebendazole show the highest cure rates, but these are usually low or only moderate (<50%) . The pressing need for developing new anthelmintic drugs, particularly for T. trichiura, cannot be emphasized enough. In addition, the therapeutically useful life span of these drugs is endangered should resistance develop and start to spread –.
The antiprotozoal drug nitazoxanide, which is marketed for the treatment of intestinal parasitic infections (i.e., Cryptosporidium parvum and Giardia intestinalis) has been reported to also have trichuricidal properties , . Silbereisen and colleagues recently showed that nitazoxanide is highly active against Trichuris muris in vitro . In clinical trials high cure rates were reported against T. trichiura as well as A. lumbricoides and hookworm, following multiple doses (200 mg for children aged below 12 years and 500 mg for patients aged 12 years and above, twice daily for 3 days) of nitazoxanide –. Hence, nitazoxanide has been listed as a potential drug candidate for human-soil transmitted helminthiasis and further research was suggested .
We report the findings of a randomized, double-blind, placebo-controlled trial, which specifically assessed the efficacy and safety of nitazoxanide given as a single dose (1,000 mg) in the treatment of T. trichiura in school-aged children on Pemba, Tanzania. The standard treatment with albendazole (400 mg) served as a benchmark. In addition, one group of children was given nitazoxanide (1,000 mg) on the first day and albendazole (400 mg) on the following day, in order to evaluate if an enhanced efficacy would be observed following this combination chemotherapy. A fourth group of children received placebo (the treatment groups are summarized in Figure 1). Since A. lumbricoides and hookworm coexist in the current setting, outcomes on these nematodes are also reported.
Flow diagram of the randomized, placebo-controlled trial assessing the efficacy of albendazole, nitazoxanide, and albendazole combined with nitazoxanide, administered separately on two consecutive days, in the treatment of Trichuris trichiura infections.
Ethical clearance was obtained from the ethics committee of Basel, Switzerland (EKBB, reference no. 225/10) and from the Ministry of Health and Social Welfare in Zanzibar (ZAMREC, reference no. 0001/010). The study is registered at Current Controlled Trials (ISRCTN08336605). Written informed consent was acquired from the children's parents or legal guardians to participate in this trial. Children assented orally. It was emphasized that study participation would be voluntary and withdrawal possible at any time.
Our trial was carried out in June and July 2011 on Pemba, one of the major islands in the Zanzibar archipelago, which belongs to Tanzania. The schools of Wawi (geographical coordinates; 5°15′22″S latitude, 39°47′28″E longitude) and Al-Sadik (5°15′42″S, 39°48′25″E), both located less than 10 km from Chake Chake, the main town of Pemba (5°14′45″S, 39°45′00″E, ∼22,000 inhabitants), were selected. In the school year 2010/2011, a total of 1,100 children were registered in Wawi and 437 in Al-Sadik. Both schools were easily accessible by car from the Public Health Laboratory–Ivo de Carneri (PHL–IdC) in Chake Chake.
Sample Size Calculation
To determine the sample size, we assumed a cure rate of 28% for single oral albendazole against T. trichiura based on data from a meta-analysis . The efficacy of single oral nitazoxanide against T. trichiura is not known. Therefore we assumed that it would be at least similar to that of albendazole (20–30%). Moreover, we hypothesized that an albendazole-nitazoxanide combination would achieve a considerably higher cure rate (50%). Monte Carlo simulations (imperfect test with a sensitivity of 90%) computed a sample size of 95 T. trichiura-infected individuals in each arm to detect a difference of single medication treatments versus both, the placebo group and the albendazole-nitazoxanide group at a significance level of 5% with 80% power. Allowing for drop outs and assuming an overall T. trichiura prevalence of 80%, we targeted approximately 125 children per treatment arm for the baseline screening.
Study Flow and Procedures
Before the onset of the study, the headmasters of Wawi and Al-Sadik were asked for permission to carry out the trial at their schools. The parents of the children were invited to the schools, so that they could be explained the purpose and procedures of the study, including potential risks and benefits. Questions could be asked in a discussion round and clarification was given to parents.
At the first day of enrolment, all children attending standards one to five received an empty stool container together with a consent form; both labeled with unique identification numbers (ID). After recording their name, sex, age, and school grade, children were invited to return the container with a fresh sample of the next morning stool together with the signed consent form. Filled stool containers and signed consent forms were collected from the children and a new empty container was handed out for collection of a second stool sample on the following day.
All children who returned a signed informed consent and had two stool samples were assigned to one of the four treatment groups, regardless of their helminths infection status. Before drug administration, all children were examined by a physician. Exclusion criteria were: (i) presence of any abnormal medical condition, judged by the study physician; (ii) history of acute or severe chronic disease (cancer, diabetes, chronic heart, liver, or renal disease); and (iii) recent use of anthelmintic drugs (within past 4 weeks). Additionally, the weight and height of all children were measured and if there was any indication of fever, axillary temperature was taken using a digital thermometer.
Three weeks posttreatment, children were asked again for two stool samples collected over consecutive days to determine the efficacy of the different treatments. At the end of the study, all children who were still infected with soil-transmitted helminths were offered a dose of albendazole (400 mg) following national guidelines , .
Randomization, Treatment, and Adverse Events
An independent statistician created a randomization code assigning to each ID a number from 1–4, representing the four treatment arms: (i) nitazoxanide (1,000 mg) plus albendazole (400 mg); (ii) nitazoxanide-matching placebo plus albendazole (400 mg); (iii) nitazoxanide (1,000 mg) plus albendazole-matching placebo; and (iv) two placebos. For blinding purposes, the tablets were packed before treatment into small plastic bags, labeled with the unique IDs. Nitazoxanide (Alinia®) and albendazole (Zentel®) tablets were the products of Romark and GlaxoSmithKline, respectively. Placebos were produced at the Department of Pharmaceutical Sciences, University of Basel by one of the authors (R.A.). During the trial all drugs were stored at room temperature, not exceeding 25°C. Since interactions between nitazoxanide and albendazole have not been studied before, the two drugs were administered on two consecutive days. Hence, on the first day of treatment, children received two tablets of nitazoxanide (500 mg each) or two nitazoxanide-matching placebos. On the second day, children received one tablet of albendazole (400 mg) or an albendazole-matching placebo. Since the trial was double-blinded, neither the child, nor the person giving the treatment knew to which treatment arm the child was allocated to.
Before treatment, children were asked if they suffer from any adverse events. Drugs were then administered with a cup of water and each child received a small snack. Three hours after treatment, adverse events were actively assessed by interviewing each child. On the following day, before receiving the second treatment, adverse events were investigated again. The same procedures were repeated 3 and 24 hours after the second treatment.
Stool samples were transferred to PHL–IdC. Duplicate Kato-Katz thick smears, using 41.7 mg templates, were prepared from each stool sample . Kato-Katz thick smears were examined under a microscope by experienced laboratory technicians within 20–40 min after preparation, as recommended to avoid over clearing of hookworm eggs . All hookworm eggs were counted. Subsequently, the slides were re-examined for T. trichiura and A. lumbricoides, with parasite eggs counted and recorded separately. To ensure high quality of the diagnosis, 10% of the slides, selected at random, were re-examined. In cases of discordant results, slides were read a third time and results discussed until agreement was reached.
Parasitological data and reported adverse events were double entered into an Excel spreadsheet and cross-checked. In case of discrepancy, the original files were consulted to correct the data entry. All statistical analyses were performed with Stata 10.1 software (StataCorp).
Cure rates were calculated as the proportion of egg-positive children at baseline, who became egg-negative after treatment. Egg counts from the four Kato-Katz thick smears were added up for each species and multiplied by a factor 6 and expressed as eggs per gram of stool (EPG). Infection intensity was classified using pre-defined cut-offs by the World Health Organization (WHO; T. trichiura light, 1–999 EPG; moderate, 1,000–9,999; and heavy, ≥10,000) . Differences among treatment arms concerning cure rates and observed adverse events were analyzed with logistic regressions.
Geometric mean egg counts were calculated for the different treatment arms before and after drug intervention to calculate the respective egg reduction rates (ERR). We also calculated the average dose (mg/kg) of each drug that the children received per treatment arm and analyzed with a logistic regression if the dose of treatment had an influence on the cure rates.
We used two different types of analyses: (i) per-protocol analysis, including only those children who had complete data records (quadruplicate Kato-Katz results before and after treatment and being treated); and (ii) available case analysis (which is sometimes erroneously referred to as an intention-to-treat analysis ) based on the treatment intent, hence analyzing data from all individuals who were assigned to one of the four treatment arms and had primary outcome data. A greater emphasis is given in our manuscript on the per-protocol analysis (available case results summarized in Table S1) since a bias might have been introduced in the available case analysis given that children absent on the first treatment day (nitazoxanide) were shifted to a later starting treatment period, while this was not possible for children missing the second treatment day (albendazole).
From the 928 children invited to participate in the study, 172 refused to participate or did not return a signed consent form. Another 47 children failed to provide two stool samples and from seven children the IDs on the stool samples were lost and hence they had to be excluded from the trial. One child received anthelmintic treatment less than 4 weeks before the onset of our trial and was therefore excluded. The remaining 701 children (549 from Wawi and 152 from Al-Sadik) were randomly assigned to one of the four treatment arms independently of their parasitological status. Of these, 124 were T. trichiura-negative and therefore excluded from the final analysis (Figure 1). Fifteen children missed the first treatment, and 14 children were absent on the second day of treatment. At follow-up, 13 children provided no or only a single stool sample and two children were excluded due to other reasons. In total 44 T. trichiura-infected children were lost during treatment and follow-up. Hence, 533 children were included in the per-protocol analysis. The loss of participants was distributed equally over the different treatment arms; the double placebo group was characterized by loss of the most participants (n = 14). Of the 29 participants not receiving treatment, all 14 who missed the second treatment provided primary end point data and could therefore be followed up; hence 547 children were included in the available case analysis.
Most of the 701 children subjected to multiple Kato-Katz thick smears readings were diagnosed positive for T. trichiura (n = 577, 82%). Infections were mainly of light intensity (94%) and only one heavy T. trichiura infection was identified. Prevalence of hookworm and A. lumbricoides were 7% and 5%, respectively, and most of these infections were of light intensity. An infection with all three helminth species was diagnosed in 11 children (1.5%). The mean age of the 701 children was 10 years (range 7–15 years). Mean age, weight, and height were comparable in all four treatment arms (Table 1). There was a similar number of boys (n = 348) and girls (n = 353) participating in the study.
Efficacy against T. trichiura
Only very low cure rates were observed regardless of whether the sequentially administered nitazoxanide-albendazole combination, albendazole, or nitazoxanide were administered. In more detail, using the per-protocol analysis, nitazoxanide combined with albendazole achieved a cure rate of 16.0% (95% confidence interval (CI), 9.7–22.4%), whereas single doses of albendazole or nitazoxanide resulted in cure rates of 14.5% (95% CI, 8.4–20.6%), and 6.6% (95% CI, 2.4–10.8%), respectively. Children receiving placebo showed an apparent cure rate of 8.9% (95% CI, 4.0–13.8%) (Table 2). Similar results were observed using the available case analysis (Table S1). Comparing the treatment outcomes using a logistic regression revealed that albendazole had a significant effect on infections with T. trichiura (odds ratio (OR), 0.47; 95% CI, 0.27–0.81; p = 0.007) while nitazoxanide showed no effect (OR, 1.04; 95% CI, 0.61–1.78; p = 0.89). There was some indication of an interaction between the two drugs (OR, 0.64; 95% CI, 0.21–1.98), however, this result was not significant (p = 0.44).
The ERR for T. trichiura was 54.9% (bootstrap 95% CI, 37.7–67.9%) for the nitazoxanide-albendazole combination, 45.6% (95% CI, 25.9–61.0%) for albendazole alone, 13.4% (95% CI, 0.0–33.7%) for nitazoxanide alone, and 17.6% (95% CI, 0.0–36.7%) for the placebo-controlled treatment arm (Table 2). Large confidence intervals indicate a high variance in ERRs. Therefore the only significant difference between the treatment arms (defined by non-overlapping bootstrap CI), was found between nitazoxanide-albendazole compared to the nitazoxanide monotherapy treatment group and the placebo-controlled treatment arm. However, even though CIs are overlapping, there seems to be a trend that albendazole alone resulted in higher ERRs.
The amount of milligrams of drug administered per kilogram of body weight ranged from 22.7 to 64.9 mg/kg for nitazoxanide and from 7.7 to 27.2 mg/kg for albendazole (Table 2). Logistic regression revealed no statistically significant association between body weight and cure rates between the different treatment arms which received an active drug.
Efficacy against Other Soil-Transmitted Helminths
Less than 10% of the children were infected with hookworm (n = 48; 7%) and A. lumbricoides (n = 31; 4%). Albendazole was highly efficacious against both parasites with cure rates of 100% against A. lumbricoides and 81.8% against hookworm (95% CI, 54.6–100%). Nitazoxanide showed moderate efficacy against those two nematode species with cure rates of 66.7% (95% CI, 35.4–98.0%) against hookworm and 62.5% (95% CI 19.2–100.0%) against A. lumbricoides (Table 2). These data, however, lacked statistical significance. Of note, placebo had an apparent cure rate against hookworm infection of 55.6%.
In total, 678 of the treated children answered a standardized questionnaire pertaining to adverse events. However, not all of these children responded at each of the five follow-up time points (Table 3). Before treatment, 28 (4.1%) children reported minor symptoms (e.g., headache and abdominal pain). After treatment (both first and second round of treatment) a total of 244 children complained at least once about minor adverse events at one of the four follow-up examinations (3 and 24 hours after each treatment). Only one child had moderate adverse events, namely headache 24 hours after receiving nitazoxanide. This child was treated with paracetamol and the headache resolved within 3 hours. In total 307 adverse events were reported after starting the treatment regimen. Abdominal cramps and headache were the most frequent ones (165 times (53.7%) and 69 times (22.5%), respectively) (Table S2). Other reported adverse events were nausea (6.8%), vertigo (5.5%), diarrhea (4.6%), fever (3.6%), allergic reaction (1.6%), vomiting (1.3%), and fatigue (0.3%).
Three hours after the first treatment, minor adverse events were reported by 101 (14.9%) participants. Children who received placebo reported significantly more about minor adverse events compared to the pretreatment situation (OR, 2.97; 95% CI, 1.50–6.21) (Table 3). Children who were given single nitazoxanide had significantly more adverse events 3 hours after treatment compared to the placebo recipients at the same time point (OR, 2.02; 95% CI, 1.28–3.24). On the next day (24 hours after the first treatment) 56 (8.3%) children reported adverse events. Participants receiving nitazoxanide still had significantly higher odds of reporting adverse events (OR, 2.49; 95% CI, 1.38–4.50). Three hours after the second treatment, children treated with albendazole did not report significantly more adverse events than placebo recipients (OR, 1.47; 95% CI, 0.59–3.70). At this time point, nitazoxanide was no longer associated with significantly more adverse events than placebo recipients (OR, 2.04; 95% CI, 0.85–4.91) and both drugs combined (treatment group 1) showed no cumulative effect regarding adverse events (OR, 0.67; 95% CI, 0.21–2.18). Twenty-four hours after the second treatment adverse events were resolved. Logistic regression revealed ORs of 0.77 (95% CI 0.35–1.71) for albendazole, 0.76 (95% CI 0.35–1.69) for nitazoxanide, and 1.40 (95% CI 0.44–4.41) for the sequentially administered nitazoxanide-albendazole combination.
Following up on the promising trichuricidal properties observed in in vitro studies , we carried out the first randomized, double-blind, placebo-controlled trial administering nitazoxanide as a single dose of 1,000 mg to T. trichiura-infected school-aged children in a highly endemic area in Pemba. In addition, since combination chemotherapy is being advocated in many therapeutic areas, as it enhances efficacy and lowers the risk of resistance development , one group of children was treated with a nitazoxanide-albendazole combination which was administered over two consecutive days.
A high single dose of nitazoxanide (1,000 mg) showed no therapeutic effect against T. trichiura. This result is in contrast to previous studies, which reported high cure rates when the drug was administered as multiple dose treatment regimen (6 times 200 mg or 500 mg) to T. trichiura-infected patients –. It is plausible that pharmacokinetic properties of “multiple doses a day” nitazoxanide are superior to “once a day” nitazoxanide in that it achieves a longer half life. However, since the global strategy targeting neglected tropical diseases advocates preventive chemotherapy (i.e., regular deworming with single oral doses), multiple dosing is currently not recommended, as it poses operational and financial challenges . A rigorous diagnostic approach as performed in this study (two times duplicate Kato-Katz thick smears before and after treatment) can lead to lower observed cure rates, since, especially light infections, are more likely to be detected . Nevertheless, two of the above mentioned studies which found high cure rates and ERRs for nitazoxanide against T. trichiura infections also collected several stool samples after treatment, and hence pursued a thorough diagnostic approach. Diagnosis, therefore, does not seem to be the main reason for the contradictory results.
The standard treatment albendazole revealed a very low cure rate against T. trichiura when given at a single dose of 400 mg, which is in agreement with the results of several previous studies , , . It is interesting to note that the ERR following albendazole treatment was still moderate (73%) in the same setting 12 years ago, but was similarly low as the ERR obtained in this trial, in a study conducted by Knopp et al. in 2009 in neighboring Unguja, Zanzibar , . This might be an indicator of tolerance or resistance development to albendazole against T. trichiura. Of note, Levecke et al.  recently showed that ERRs can differ strongly between individual settings and that albendazole has higher ERRs in settings with low infection intensities. Our trial could not confirm this hypothesis since albendazole achieved only a low ERR in children characterized by low infection intensities.
The combination of albendazole and nitazoxanide had slightly, though not significantly higher cure rates and ERRs than albendazole alone. Since drug interactions have not been evaluated for this combination, drugs were administered on subsequent days. One disadvantage of spacing the drug is that synergistic effects might be missed. On the other hand, a recent study which examined the effect of a simultaneous nitazoxanide-albendazole combination against adult T. muris in vitro detected an antagonistic effect .
Only a few children were (co)-infected with hookworm and/or A. lumbricoides. Nonetheless, these data illustrate that the standard treatment albendazole has a high efficacy against these parasites. The good activity against these two helminths and low efficacy against T. trichiura is also supported by the baseline prevalences (T. trichiura (82.2%), hookworm (6.8%), and A. lumbricoides (4.6%)) observed in the current trial. The settings where the study was conducted (Wawi and Al-Sadik schools) are part of the annual deworming in Zanzibar and are therefore regularly treated with albendazole.
The placebo-controlled treatment group had a cure rate of 55.6% against hookworms. This finding might indicate that the diagnostic tool used to detect hookworm eggs in this study was not sufficiently sensitive. One reason might be that subjects with light infections may only shed very few or sometimes no eggs, resulting in a negative Kato-Katz test result , . To overcome this problem in future studies it might be advisable to use an additional diagnostic technique with higher sensitivity such as the FLOTAC technique, which allows using a larger amount of stool, or indirect diagnostic technique such as multiplex real-time PCR , –.
We observed a high frequency of adverse events, but these were mostly mild, were, at times, already reported before treatment, and also by placebo recipients ; and hence were not consistently treatment related. Nevertheless, 3 and 24 hours after the first day of treatment (administration of nitazoxanide or a nitazoxanide-matching placebo) children treated with nitazoxanide reported significantly more adverse events compared to those who had received placebo. This increase in adverse events was not observed after the second day of treatment (children treated with albendazole suffered from a similar number of adverse events episodes than children who had obtained placebo), suggesting that the standard treatment albendazole triggers less adverse events than nitazoxanide. Adverse events related to treatment were resolved 24 hours after the second treatment, and the highest number of adverse events was reported from placebo-treated children.
In conclusion, a single oral dose of nitazoxanide cannot be recommended for the treatment of infection with T. trichiura since we observed low cure rate and ERR as well as significantly more adverse events than the standard drug albendazole. Note that, nitazoxanide is also much more expensive than the benzimidazoles, pyrantel pamoate, or levamisole. Moreover, also albendazole showed a low efficacy against T. trichiura in our study setting which did also not significantly improve by adding nitazoxanide on the next treatment day. Therefore the discovery and development of novel anthelmintic drugs, in particular against infections with T. trichiura, has a high priority.
Effect of albendazole, nitazoxanide, sequentially administered albendazole-nitazoxanide combination, and placebo against soil-transmitted helminths calculated with available-case analysis.
Number of specific adverse events assessed at different time points.
We are grateful to the children attending Wawi and Al-Sadik schools for participating in this trial. We thank all the teachers and headmasters from both schools for their great support. We express our thanks to the whole team from the Public Health Laboratory–Ivo de Carneri, in Pemba for their work in the field and in the laboratory. Dr. Tracy Glass is acknowledged for her assistance with the randomization and Ms. Chiara Di for her help in the field.
Conceived and designed the experiments: JK MA JU JH BS S. Ame. Performed the experiments: BS S. Ame JK S. Ali MA. Analyzed the data: BS JH. Contributed reagents/materials/analysis tools: RA. Wrote the paper: BS JK JU JH MA S. Ame S. Ali RA.
- 1. Chan MS (1997) The global burden of intestinal nematode infections–fifty years on. Parasitol Today 13: 438–443.
- 2. Hotez PJ, Molyneux DH, Fenwick A, Ottesen E, Ehrlich Sachs S, et al. (2006) Incorporating a rapid-impact package for neglected tropical diseases with programs for HIV/AIDS, tuberculosis, and malaria. PLoS Med 3: e102.
- 3. Bethony J, Brooker S, Albonico M, Geiger SM, Loukas A, et al. (2006) Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm. Lancet 367: 1521–1532.
- 4. Pullan RL, Brooker SJ (2012) The global limits and population at risk of soil-transmitted helminth infections in 2010. Parasites & vectors 5: 81. doi:10.1186/1756-3305-5-81.
- 5. Albonico M, Chwaya HM, Montresor A, Stolfzfus RJ, Tielsch JM, et al. (1997) Parasitic infections in Pemba Island school children. East Afr Med J 74: 294–298.
- 6. Warren KS (1988) Hookworm control. Lancet 332: 897–898.
- 7. Albonico M, Crompton DWT, Savioli L (1999) Control strategies for human intestinal nematode infections. Adv Parasitol 42: 277–341.
- 8. WHO (2010) 2nd WHO model list of essential medicines for children (March 2010 update).
- 9. Horton J (2003) Human gastrointestinal helminth infections: are they now neglected diseases? Trends Parasitol 19: 527–531.
- 10. Keiser J, Utzinger J (2010) The drugs we have and the drugs we need against major helminth infections. Adv Parasitol 73: 197–230.
- 11. Peldan K, Pitkanen T (1982) Treatment of Trichuris trichiura infection with a single dose of oxantel pamoate. Scand J Infect Dis 14: 297–299.
- 12. Albonico M, Bickle Q, Haji HJ, Ramsan M, Khatib KJ, et al. (2002) Evaluation of the efficacy of pyrantel-oxantel for the treatment of soil-transmitted nematode infections. Trans R Soc Trop Med Hyg 96: 685–690.
- 13. Rajasekariah GR, Deb BN, Jones MP, Dhage KR, Bose S (1991) Response of pre-adult and adult stages of Trichuris muris to common anthelmintics in mice. Int J Parasitol 21: 697–702.
- 14. Hemphill A, Mueller J, Esposito M (2006) Nitazoxanide, a broad-spectrum thiazolide anti-infective agent for the treatment of gastrointestinal infections. Expert Opin Pharmacother 7: 953–964.
- 15. Rossignol JF, Cavier R (1975) New derivative of 2-benzamido-5-nitrothiols. Chemical Abstracts 83: 28216.
- 16. Silbereisen A, Tritten L, Keiser J (2012) Exploration of novel in vitro assays to study drugs against Trichuris spp. J Microbiol Methods 87: 169–175.
- 17. Abaza H, El-Zayadi AR, Kabil SM, Rizk H (1998) Nitazoxanide in the treatment of patients with intestinal protozoan and helminthic infections: a report on 546 patients in Egypt. Curr Ther Res Clin Exp 59: 116–121.
- 18. Romero Cabello R, Guerrero LR, Munoz Garcia MR, Geyne Cruz A (1997) Nitazoxanide for the treatment of intestinal protozoan and helminthic infections in Mexico. Trans R Soc Trop Med Hyg 91: 701–703.
- 19. Juan JO, Lopez Chegne N, Gargala G, Favennec L (2002) Comparative clinical studies of nitazoxanide, albendazole and praziquantel in the treatment of ascariasis, trichuriasis and hymenolepiasis in children from Peru. Trans R Soc Trop Med Hyg 96: 193–196.
- 20. Diaz E, Mondragon J, Ramirez E, Bernal R (2003) Epidemiology and control of intestinal parasites with nitazoxanide in children in Mexico. Am J Trop Med Hyg 68: 384–385.
- 21. Keiser J, Utzinger J (2008) Efficacy of current drugs against soil-transmitted helminth infections: systematic review and meta-analysis. JAMA 299: 1937–1948.
- 22. Katz N, Chaves A, Pellegrino J (1972) A simple device for quantitative stool thick-smear technique in schistosomiasis mansoni. Rev Inst Med Trop São Paulo 14: 397–400.
- 23. Martin LK, Beaver PC (1968) Evaluation of Kato thick-smear technique for quantitative diagnosis of helminth infections. Am J Trop Med Hyg 17: 382–391.
- 24. Montresor A, Crompton DWT, Hall A, Bundy DAP, Savioli L (1998) Guidelines for the evaluation of soil-transmitted helminthiasis and schistosomiasis at community level: a guide for managers and control programs. Geneva: World Health Organization, WHO/CTS/SIP 98.1.
- 25. Higgins JP, Deeks JJ, Altman DD (2008) Cochane Statistical Methods Group: chapter 16: special topics in statistics. Available: http://hiv.cochrane.org/sites/hiv.cochrane.org/files/uploads/Ch16_Specialstatistics.pdf. Accessed 2012 Feb 22.
- 26. Gilles HM, Hoffman PS (2002) Treatment of intestinal parasitic infections: a review of nitazoxanide. Trends Parasitol 18: 95–97.
- 27. Hotez P, Raff S, Fenwick A, Richards F, Molyneux DH (2007) Recent progress in integrated neglected tropical disease control. Trends Parasitol 23: 511–514.
- 28. Knopp S, Speich B, Hattendorf J, Rinaldi L, Mohammed KA, et al. (2011) Diagnostic accuracy of Kato-Katz and FLOTAC for assessing anthelmintic drug efficacy. PLoS Negl Trop Dis 5: e1036.
- 29. Albonico M, Smith PG, Hall A, Chwaya HM, Alawi KS, et al. (1994) A randomized controlled trial comparing mebendazole and albendazole against Ascaris, Trichuris and hookworm infections. Trans R Soc Trop Med Hyg 88: 585–589.
- 30. Knopp S, Mohammed KA, Speich B, Hattendorf J, Khamis IS, et al. (2010) Albendazole and mebendazole administered alone or in combination with ivermectin against Trichuris trichiura: a randomized controlled trial. Clin Infect Dis 51: 1420–1428.
- 31. Levecke B, Mekonnen Z, Albonico M, Vercruysse J (2012) The impact of baseline faecal egg counts on the efficacy of single-dose albendazole against Trichuris trichiura. Trans R Soc Trop Med Hyg 106: 128–130.
- 32. Tritten L, Silbereisen A, Keiser J (2012) Nitazoxanide: in vitro and in vivo drug effects against Trichuris muris and Ancylostoma ceylanicum, alone or in combination. Int J Parasitol Drugs Drug Resist 2: 98–105.
- 33. Knopp S, Rinaldi L, Khamis IS, Stothard JR, Rollinson D, et al. (2009) A single FLOTAC is more sensitive than triplicate Kato-Katz for the diagnosis of low-intensity soil-transmitted helminth infections. Trans R Soc Trop Med Hyg 103: 347–354.
- 34. Booth M, Vounatsou P, N'Goran EK, Tanner M, Utzinger J (2003) The influence of sampling effort and the performance of the Kato-Katz technique in diagnosing Schistosoma mansoni and hookworm co-infections in rural Côte d'Ivoire. Parasitology 127: 525–531.
- 35. Cringoli G, Rinaldi L, Maurelli MP, Utzinger J (2010) FLOTAC: new multivalent techniques for qualitative and quantitative copromicroscopic diagnosis of parasites in animals and humans. Nat Protoc 5: 503–515.
- 36. Utzinger J, Rinaldi L, Lohourignon LK, Rohner F, Zimmermann MB, et al. (2008) FLOTAC: a new sensitive technique for the diagnosis of hookworm infections in humans. Trans R Soc Trop Med Hyg 102: 84–90.
- 37. Glinz D, Silué KD, Knopp S, Lohourignon LK, Yao KP, et al. (2010) Comparing diagnostic accuracy of Kato-Katz, Koga agar plate, ether-concentration, and FLOTAC for Schistosoma mansoni and soil-transmitted helminths. PLoS Negl Trop Dis 4: e754.
- 38. Verweij JJ, Brienen EAT, Ziem J, Yelifari L, Polderman AM, et al. (2007) Simultaneous detection and quantification of Ancylostoma duodenale, Necator americanus, and Oesophagostomum bifurcum in fecal samples using multiplex real-time PCR. Am J Trop Med Hyg 77: 685–690.
- 39. Macedo A, Farré M, Baños JE (2003) Placebo effect and placebos: what are we talking about? Some conceptual and historical considerations. Eur J Clin Pharmacol 59: 337–342.