NCT Number: NCT00140361
Efficacy of Sulphadoxine-pyrimethamine and Artemisinin-containing Combination Therapy for Malaria
This is an ongoing monitoring activity of efficacy of sulfadoxine-pyrimethamine (SP), which is the current national treatment of choice for uncomplicated malaria in Tanzania, and a combination of SP and artesunate among children < 5 years in 3 sites in rural Tanzania.
Protocol was amended in 2004 to (1) include lumefantrine+artemether, the newly identified first-line treatment for malaria to be introduced into Tanzania in 2006; (2) on a limited basis, include adult patients; (3) extend follow-up to 28 days; (4) investigate whether treated bednets would reduce confounding by reinfection
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Ngere Ngere Health Center, Ngerengere, Morogoro Rural, Tanzania
About this study
This is an ongoing monitoring activity of efficacy of sulfadoxine-pyrimethamine (SP), which is the current national treatment of choice for uncomplicated malaria in Tanzania, and a combination of SP and artesunate among children < 5 years in 3 sites in rural Tanzania.
Protocol was amended in 2004 to (1) include lumefantrine+artemether, the newly identified first-line treatment for malaria to be introduced into Tanzania in 2006; (2) on a limited basis, include adult patients; (3) extend follow-up to 28 days; (4) investigate whether treated bednets would reduce confounding by reinfection
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Children < 5 years of age (in one site, patients of all ages are eligible).
Documented fever (axillary temperature >= 37.5oC) in the absence of another obvious cause of fever or other serious or chronic medical condition
Unmixed infection with P. falciparum of between 2,000 and 250,000 asexual parasites/mm3
Patients' or the patients' parent's or guardian's informed consent and willingness to participate in the study
Exclusion criteria
Any evidence of severe malaria that would require hospitalization for treatment.
Reported allergy to any antimalarial drugs, including sulfa and artemisinin drugs.
History of pregnancy or delayed menstrual period
Breastfeeding a child less than 8 weeks of age
Treatment and study plan
sulfadoxine-pyrimethamine plus artesunate
Druglumefantrine plus artemether
DrugSleeping under insecticide-treated bednet
BehavioralPrimary outcomes
-
Clinical and parasitologic failure rate
Sponsors and collaborators
Lead sponsor
Centers for Disease Control and Prevention
Fed
Collaborators
- United States Agency for International Development (USAID)
Registry information
Official study title
Assessing and Monitoring the Efficacy of Sulfadoxine/ Pyrimethamine (SP) and the Combination of SP Plus Artesunate for Uncomplicated Malaria Infections Among Children
Important dates
- Study start
- 2000
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Sep 1, 2005
- Registry last updated
- Sep 11, 2012
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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