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. 2006 Jan 25;2006(1):CD004966. doi: 10.1002/14651858.CD004966.pub2

Dorsey 2002.

Methods Randomized placebo controlled trial
Generation of allocation sequence: computer‐generated randomization list
Allocation concealment: not mentioned
Blinding: participants and study investigators blinded
Inclusion of all randomized participants: no (93/122)
Length of follow up: 14 days
Participants Number: 211 children enrolled
Inclusion criteria: children 6 months to 5 years old; no history of treatment for malaria in previous 2 weeks or fever in last 48 h; no history of adverse reactions to any of the study drugs; no history of sickle cell disease; haemoglobin 50 g/L or more; willingness to remain in the city of Kampala and follow the study protocol for the next 12 months; parent or guardian written informed consent
Interventions 1. Sulfadoxine‐pyrimethamine (SP) plus amodiaquine (AQ)
 2. SP plus artesunate (AS)
AQ: 10 mg/kg/day for 2 days and 5 mg/kg for 1 day
AS: 4 mg/kg/day for 3 days
SP: 25 mg/kg sulfadoxine and 1.25 mg/kg pyrimethamine; single dose
Third arm not relevant to review: SP plus vitamin C placebo
Outcomes 1. Treatment failure at day 14 and 28; at day 28 both adjusted and unadjusted for new infections 
 2. Mentions adverse events but did not report any
 3. Parasite carriage reported for episodes not patients
 3. Presence of fever
 4. Mentioned adverse events but did not give details by treatment arm
Notes Location: Mulago Hospital, Kampala, Uganda
Date: July 2000 to August 2001
Follow up was 14 days for each episode of malaria over 1‐year period
Funding: Fogarty International Center/National Institutes of Health and the UNDP/World Bank/World Health Organization (WHO) Special Programme for Research and Training in Tropical Diseases (TDR)