Malaria Journal

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Open Access Research

Randomized clinical trial of artemisinin versus non-artemisinin combination therapy for uncomplicated falciparum malaria in Madagascar

Didier Ménard1*, Nohary NH Andrianina1, Zakaherizo Ramiandrasoa1, Arthur Randriamanantena2, Noéline Rasoarilalao1, Martial Jahevitra1, Arsène Ratsimbasoa2, Luciano Tuseo3 and Andrianirina Raveloson4

Author Affiliations

1 Malaria Unit Research, Institut Pasteur de Madagascar, BP 1274, Antananarivo 101, Madagascar

2 Epidemiology Unit, Institut Pasteur de Madagascar, Antananarivo 101, Madagascar

3 Roll Back Malaria, WHO Office of Madagascar and La Réunion, Antananarivo 101, Madagascar

4 National Malaria Control Programme, Ministry of Health, Antananarivo 101, Madagascar

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Malaria Journal 2007, 6:65 doi:10.1186/1475-2875-6-65

Published: 22 May 2007

Abstract

Background

Data concerning antimalarial combination treatment for uncomplicated malaria in Madagascar are largely lacking. Randomized clinical trial was designed to assess therapeutic efficacies of chloroquine (CQ), amodiaquine (AQ), sulphadoxine-pyrimethamine (SP), amodiaquine plus sulphadoxine-pyrimethamine combination (AQ+SP) and artesunate plus amodiaquine combination (AQ+AS).

Methods

287 children between 6 months and 15 years of age, with uncomplicated falciparum malaria, were enrolled in the study. Primary endpoints were the day-14 and day-28 risks of parasitological failure, either unadjusted or adjusted by genotyping.

Results

All treatment regimens, except for CQ treatment, gave clinical cure rates above 97% by day-14 and 92% by day-28 (PCR-corrected). AQ+SP was as effective as AQ+AS. The risk of new infection within the month after therapy was generally higher for AQ+AS than AQ+SP.

Conclusion

These findings show that the inexpensive and widely available combination AQ+SP may be valuable in for the treatment of uncomplicated malaria in Madagascar and could have an important role in this country, where much of the drugs administered go to patients who do not have malaria.