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Comparison of Praziquantel with antimalarial drug combinations in the treatment of children with bilharzia in Kirinyaga county, Kenya

Phase 3
Completed
Conditions
schistosomiasis
Registration Number
PACTR202001919442161
Lead Sponsor
Kenya Medical Research Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
540
Inclusion Criteria

For participants to be enrolled in the study they have to meet ALL of the following criteria:
•Aged between 6 and 15 years old (confirmed from the date of birth recorded on the school registers),
•Testing positive for S. mansoni infection (confirmed by presence of eggs in stool).
•Residing in Mwea East and Mwea West, Kirinyaga County
•Able to take oral treatment
•Respective parent/ guardian provides written informed consent for the child to participate in the study
•Child provides written assent to participate in the study

Exclusion Criteria

Potential participants will be excluded for any of the following reasons:
•Weighing more than 50 kg,
•Haemoglobin level = 5.0g/dL
•Signs of severe malnutrition (defined as severe wasting or MUAC <12cm)
•Hypersensitivity to Artesunates, sulfonamides or praziquantel.
•Use of an anti-malaria or anti-schistosomial drug within 28 days before enrollment in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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