Malaria Clinical Trial
Official title:
Efficacy of Artesunate-amodiaquine, Dihydroartemisinin-piperaquine and Artemether-lumefantrine Combination Therapies for the Treatment of Uncomplicated Plasmodium Falciparum Malaria in Children Aged 6 to 59 Months in Maradi, Niger 2012-13
Study treatments:
- Artemether-lumefantrine
- Artesunate-amodiaquine
- Dihydroartemisinin-piperaquine
Location:
Maradi, Niger
Principal Objective:
To measure the clinical and parasitological efficacy of the three artemisinin combination
therapies over a period of 42 days from the start of treatment and with polymerase chain
reaction assay (PCR) adjustment.
Secondary objectives:
- To determine the blood concentration of the non-artemisinin component of the treatment
(lumefantrine, desethylamodiaquine or piperaquine) at day 7
- To assess the incidence of adverse events during the follow-up period;
- To measure speed of parasite clearance
Methods:
In vivo non comparative study as for WHO standardised protocol. The study also measure the
concentration of the non-artemisinin component.
Target population:
Children under 5 years of age consulting the integrated health centres of Andoumé and
Dix-sept portes in Maradi.
Sample size:
221 patients per study treatment; 663 patients in total.
Treatment allocation:
Random.
Outcomes:
- Early treatment failure,
- Late clinical failure,
- Late parasitological failure,
- Adequate clinical and parasitological response.
Analysis:
- Cumulative success or failure rate (Kaplan-Meier analysis).
- Proportions of early treatment failures, late clinical failures, late parasitological
failures, and adequate clinical and parasitological response (called also Per-protocol
analysis).
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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