Azithromycin as Adjunctive Treatment for Uncomplicated Severe Acute Malnutrition

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age6-59
SponsorUniversity of California, San Francisco

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Azithromycin

    Drug

    oral azithromycin (20 mg/kg, single directly observed dose, oral suspension),

  • Amoxicillin

    Drug

    Standard 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 intervention

    A 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

3,000 Participants
are divided into 3 treatment groups
Group A: AzithromycinExperimental treatment 1 intervention
Group B: AmoxicillinActive comparator 1 intervention
Group C: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Weight Gain

This will be measured as weight gain in g/kg/day at 8 weeks from enrollment.

Time frame
8 weeks

Secondary outcomes

1

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.

Time frame
12 weeks
2

Number of Transfer to inpatient care

Children will be transferred to inpatient care if they develop medical complications, or their condition deteriorates.

Time frame
12 weeks
3

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.

Time frame
12 months

Other outcomes

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