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Protocol
|Research Protocol

Efficacy of amodiaquine-artesunate and artemether-lumefantrine for the treatment of uncomplicated childhood plasmodium falciparum malaria

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Abstract
PRIMARY OBJECTIVES of study:
To compare the in vivo efficacy of artesunate-amodiaquine (ASAQ) versus artemether-lumefantrine (Coartem®) in a population of children aged between 6 and 59 months suffering from uncomplicated P. falciparum malaria. This will be expressed as the PCR genotyping corrected rates of parasite clearance as a measure of efficacy at day 42 after initiation of anti-malarial therapy (the correction is for recrudescence versus re-infection). This will provide the MoH with evidence for the most appropriate choice of ACT for this region.
SECONDARY OBJECTIVES:
- To measure the PCR uncorrected efficacy of both drugs at day 42 after treatment initiation
- To measure the PCR corrected and uncorrected efficacy of both drugs at days 14 and 28 after treatment initiation
- To calculate the proportion of early therapeutic failures, late clinical failures and late parasitological failures in a period of 42 days after treatment initiation
- To formulate recommendations and to enable the Ministry of Health to make informed decisions about

Subject Area

malariavector borne diseases

Languages

English
Published Date
01 Jun 2014
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Efficacy of amodiaquine-artesunate and artemether-lumefantrine for the treatment of uncomplicated childhood plasmodium falciparum malaria | Protocol / Research Protocol | MSF Science Portal