CompletedPhase 4NCT02590627
In-vivo Efficacy and Safety of Artemether/Lumefantrine Vs Dihydroartemisinin-piperaquine for Treatment of Uncomplicated Malaria and Assessment of Parasite Genetic Factors Associated With Parasite Clearance or Treatment Failure
Studying Malaria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- National Institute for Medical Research, Tanzania
- Principal Investigator
- Deus Ishengoma, PHDNational Institute for Medical Research
- Intervention
- Artemether-lumefantrine(drug)
- Enrollment
- 509 target
- Eligibility
- 10 years · All sexes
- Timeline
- 2014 – 2015
Study locations (2)
- Ujiji Health Centre, Ujiji, Kigoma Region, Tanzania
- Muheza Disignated District Hospital, Muheza, Tanga, Tanzania
Collaborators
Ministry of Health and Social Welfare, Tanzania · World Health Organization
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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