Anti-Malarial Drug Resistance in Cameroon
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|ClinicalTrials.gov Identifier: NCT00146718|
Recruitment Status : Completed
First Posted : September 7, 2005
Last Update Posted : January 12, 2017
|Condition or disease||Intervention/treatment||Phase|
|Malaria||Drug: Amodiaquine and Sulphadoxine/Pyrimethamine||Phase 2 Phase 3|
The objectives of this study are:- .
- to evaluate the therapeutic efficacy of amodiaquine(AQ), Fansidar(SP) and the combination amodiaquine/Fansidar in three sites in Cameroon namely, Garoua (Sahel-savanna), Yaounde (Forest-savannah mosaic) and Limbe (Littoral-forest)
- to determine the prevalence of molecular markers associated with resistance to chloroquine,AQ,and SP in Limbe and Garoua and of mefloquine in Yaounde.
- to investigate biological factors that may enhance anti-malaria therapeutic efficacy. This will involve an exploratory, pilot study conducted during the second year of the program.
Patients will be rapidly screened for temperature and sent to the laboratory to determine the presence or absence of malaria parasites. The patients will then be examined clinically for inclusion or exclusion. Consent will be sort from the parents and the children randomised and assigned study numbers. To avoid bias in assigning the patients to groups and to ensure equal numbers in the treatment groups, blocked randomization will be performed, using a table of random variables of varying block sizes. The physician is blinded to what treatment the patient gets.
Amodiaquine will be administered at 10mg/kg on each of the three days to children in the AQ treatment group, together with Fansidar dummy tablets. Fansidar will be given at 25 mg/kg on day 0 and quinine as rescue drug at 10mg/kg per 8H for 6 days. For the AQ/SP combination, on D0, patients will be given both 25 mg/kg SP and 10mg/kg AQ. On subsequent days the AQ or its dummy tablets(SP arm) will be given.
Clinical assessment during the study will include: physical examination and monitoring of vital signs on D0, D3, D7, D14 and D28. Hematological measurements will include: blood films, haemoglobin,glucose,blood drug levels,and baseline haematology. A maximum of 3ml of blood will be withdrawn from the patients in Yaoundé for complete analyses(see below). For patients recruited at Limbe and Garoua only finger prick blood filter paper samples will be obtained.
Day 0 blood samples (3mL) will be collected aseptically by venepuncture before therapy from each of 50 patients in Yaoundé using acid-citrate-dextrose buffer (ACD) as anticoagulant. This will be processed to provide plasma for immunological determinations and for haematology and blood drug level determinations.
The molecular characterization of diversity and mutations:
- the genetic heterogeneity of the study population will be established using primers for msp1 and msp2 shown previously to distinguish between strains.
- PCR products will be digested with restriction enzyme (RFLP-PCR) for pyrimethamine resistance genes dhfr and dhps, and for chloroquine resistant strains of the pfcrtgene.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||755 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Anti-malarial Drug Resistance in Cameroon: Therapeutic Efficacy and Biological Markers of Resistance|
|Study Start Date :||August 2003|
|Estimated Study Completion Date :||May 2005|
- Adequate clinical and parasitological response(ACPR) on Day 28
- ACPR Day 14
- Early treatment failure, between days 1 and 3
- Late treatment failure, between days 4 and 14
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00146718
|Principal Investigator:||Wilfred Mbacham, ScD||Laboratory for Public Health Biotechnology, University of Yaounde I|