Legesse 2004.
| Methods |
Design: parallel group randomized trial Duration of study: March 2003 Follow‐up: 21 days |
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| Participants |
Country: Ethiopia Setting: school Number included in study: 661 Age: 6–19 years (mean 10.6 years) Sex: female 254, male 280 Inclusion criteria: did not receive any anthelmintic drugs in the past 3 months; positive for ≥ 1 helminth infections Exclusion criteria: not reported Lost at follow‐up: 127 (19.2%) Number positive for A lumbricoides: 432 Number included in review: 432 |
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| Interventions |
Treatment strategy: screening and treat all included participants
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| Outcomes |
Outcomes included:Ascaris prevalence pre‐ and post‐treatment, cure rates, pre‐ and post‐treatment GM epg, ERR Outcomes not included in review: anthelmintic efficacy for Trichuris andS mansoni |
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| Notes |
Diagnostic technique: Kato‐Katz Funding support: mebendazole donated by Dr AR Hashim, Manager of East African Pharmaceuticals in Addis Ababa. |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Quote: "A sequentially numbered list of students positive for at least one of the two helminth infections (Ascariasis or Trichuriasis) was prepared and randomly divided into four treatment groups using random numbers obtained from a random number table." |
| Allocation concealment (selection bias) | Unclear risk | Details not reported. |
| Blinding of participants and personnel (performance bias) All outcomes | High risk | Different treatment schedule. |
| Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Details not reported. |
| Incomplete outcome data (attrition bias) All outcomes | High risk | 127 (19.2%) participants lost at follow‐up and not included in analysis. Balanced lost among groups. |
| Selective reporting (reporting bias) | High risk | Adverse events not reported. |
| Other bias | Low risk | No other obvious source of bias. |