Artemisinin-Based Combination Therapy: Clinical Trials in Cameroon

• Outpatients will be screened for malaria by blood film examination
• Malaria-positive children will be examined by the physician for inclusion or exclusion(see below)
• Informed consent will be sought from the guardians of potential patients
• Patients or guardians will be interviewed and a case record form completed
• Patients will be randomized into one of the two arms in the ratio 4:1 AQ/Art: CoArtem and issued a study card
• Filter paper and 5ml venous blood samples will be collected
• Patients will be hospitalised for three days to allow completion of therapy under observation
• The patient will be asked to return on days 7, 14 and 28 for assessment of clearance or recrudescence of parasites
• Patient will be examined for parasites and evaluated for early treatment failure (ETF), late treatment failure (LTF), late parasitological failure (LPF) or adequate clinical and parasitological response.(ACPR).
• If a patient does not appear for follow up, a community health worker will try to trace them and will collect blood onto filter paper and a microscope slide should the patient have a temperature ≥ 37.5°C
• Patients whose parents opt out of the study will be administered quinine sulphate if parasitaemic
• Filter paper samples will be air dried and stored with dessicant until required.
• Whole blood samples collected into citrate as anticoagulant will be processed for plasma, aliquoted into 300µl lots and stored at -70°C.
• Patient information will be entered at the close of each day into laptops and collectively sent to Yaounde at the end of the first month of study and thereafter at the end of each week, along with the hard copies of the case report forms.
• Analysis will be performed on the samples within three months of collection for molecular markers of resistance, genetic structure of parasites and for blood drug levels of medications used in the trial

Inclusion criteria

• children aged 6-120 months;
• axillary temperature ≥ 37.5°C and/or history of fever within past 24 hours;
• P. falciparum asexual parasitemia between 1000 and 100000/µl;
• ability to attend follow-up visits.

Exclusion criteria

• co-infections;
• underlying chronic disease;
• severe malaria as indicated by hyperparasitemia, severe anemia (PCV 15%, Hb 5g/ml), respiratory distress, inability to drink, persistent vomiting in past 24 hours;
• recent history of multiple convulsions;
• jaundice;
• the inability to stand or sit;
• history of allergy to study drugs.