Andoumé Health Centre
Maradi, Maradi Region, Niger
NCT Number: NCT01755559
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).
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Notify Me6 month–59 month
All sexes
Interventional
Phase 4
Maradi, Maradi Region, Niger
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
antimalarial ACT
Other names: AS-AQ Winthrop® Sanofi Aventis
antimalarial ACT
Other names: Euratesim, Sigma-Tau
antimalarial ACT
Other names: Coartem, Novartis
Time frame: 42 days after treatement start
Absence of parasitaemia on day 42, irrespective of axillary temperature, in patients who did not previously meet any of the criteria of early treatment failure, late clinical failure or late parasitological failure.
Time frame: 1 to 3 days after tratment start
Time frame: from day 4 to day 42 after treatment start
Time frame: from day 7 to day 42 after treatment start
Epicentre
Other
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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