This study will assess the impact of 2-drug (DA) or 3-drug (IDA) regimens on lymphatic filariasis infection parameters in communities. Parameters measured will include: circulating filarial antigenemia (CFA) assessed with the Filariasis Test Strip (FTS), antifilarial antibodies tested with plasma and microfilaremia (assessed by night blood smears and microscopy).
Age range
5 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of participants with circulating filarial antigenemia (CFA) as measured by the Filaria Test Strip
Timeframe: One sample collected about 12 months after exposure to treatment
Number of participants with IgG4 antifilarial antibodies in plasma
Timeframe: One sample collected about 12 months after exposure to treatment
Number of participants with microfilaremia as measured with night blood smear testing
Timeframe: One sample collected about 12 months after exposure to treatment