About this trial
Amoxicillin is recommended by the World Health Organization (WHO) as adjunctive therapy for the treatment of uncomplicated severe acute malnutrition (SAM). Because children with uncomplicated SAM may have asymptomatic infection due to immune suppression, presumptive treatment with a broad-spectrum antibiotic may be beneficial by clearing any existing infection and improving outcomes. Two randomized placebo-controlled randomized trials have evaluated amoxicillin for uncomplicated SAM and have found conflicting results. These results may indicate either that antibiotics are not helpful for the management of uncomplicated SAM, or that a better antibiotic is needed. Recently, the investigators demonstrated that biannual mass azithromycin distribution as a single oral dose reduces all-cause child mortality in sub-Saharan Africa. Children with uncomplicated SAM, who have an elevated risk of mortality relative to their well-nourished peers, may particularly benefit from presumptive azithromycin treatment. Our pilot data demonstrated feasibility in rapid enrollment of children with uncomplicated SAM in our study area, and showed no significant difference between azithromycin and amoxicillin, demonstrating equipoise for a full-scale trial. Here, the investigators propose an individually randomized trial in which children will be randomized to a) azithromycin, b) amoxicillin, or c) placebo, and evaluated for differences in weight gain, nutritional recovery, and the gut microbiome. The results of this study will strengthen the evidence base for policy related to the use of antibiotics as part of the management of uncomplicated SAM, including additional evidence of amoxicillin versus placebo as well as evaluation of an antibiotic class that has not been considered for uncomplicated SAM, which may lead to changes in guidelines for treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 6-59 months
WHZ<-3 SD or MUAC<115 mm
Primary residence within a catchment area of an enrollment site
Available for full 8-week study (primary endpoint)
Disqualifiers
Age less than 6 month or more than 59 months
WHZ>-3 SD or MUAC>115 mm
Primary residence is not within a catchment area of an enrollment site
Not Available for full 8-week study (primary endpoint)
Trial design
Parallel
Treatments tested in this trial
Azithromycin
Drugoral azithromycin (20 mg/kg, single directly observed dose, oral suspension),
Amoxicillin
DrugStandard of Care. A 7-day, twice-daily course of amoxicillin will be offered as a syrup to children (80 mg/kg divided into twice-daily doses, estimated with weight-based dosing).
Placebo
Other interventionA 7-day, twice-daily course of placebo will be offered as a syrup to children (80 mg/kg divided into twice-daily doses, estimated with weight-based dosing).
Treatment groups
Trial outcomes
Primary outcomes
Weight Gain
This will be measured as weight gain in g/kg/day at 8 weeks from enrollment.
Secondary outcomes
Time for Nutritional recovery
Nutritional recovery will be defined as per Burkinabé national guidelines: weight-for-height z score (WHZ) ≥ -2 on two consecutive visits and no acute complication or edema for the past 7 days OR mid-upper arm circumference (MUAC)≥ 125mm on two consecutive visits and no acute complication or edema for the past 7 days. The criterion chosen to define recovery is the same as the one used to admit the child to the program.
Number of Transfer to inpatient care
Children will be transferred to inpatient care if they develop medical complications, or their condition deteriorates.
Mortality
Vital status will be assessed at all scheduled follow-up time points, and the child's vital status (alive, died, defaulted, unknown) will be recorded in the study's mobile application.
Sponsors and contacts
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University of California, San Francisco
Lead sponsor
Centre de Recherche en Sante de Nouna, Burkina Faso
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator