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Phase 4 N=449 Randomized Quadruple-blind Treatment

Gut and Azithromycin Mechanisms in Infants and Children II

Malaria

Enrolled (actual)
449
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcome: Primary: Malaria Status — 18; 16 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Azithromycin (Drug); Placebo (Drug)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
University of California, San Francisco
Primary completion
Jun 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Malaria Status
18; 16
SECONDARY
Clinical Malaria
6; 6

Summary

Childhood mortality is decreasing worldwide. However, many sub-Saharan countries still have high children under 5 mortality rates. The MORDOR trial in Niger, Tanzania, and Malawi demonstrated a near 14% decrease in all-cause child mortality following biannual azithromycin in children 1-59 months. Current trials in Burkina aim to replicate these results from the MORDOR study with mass azithromycin treatment. The investigators conducted an individually randomized placebo-controlled trial in Burkina Faso called the Gut and Azithromycin Mechanisms in Infants and Neonates Trial (GAMIN: NCT03676751) to evaluate the effect of a single dose of azithromycin (20 mg/kg) on potential mediators of the effect of azithromycin on all-cause mortality and to evaluate changes in the gut microbiome longitudinally (results pending). Here, the investigators propose to conduct an expansion of the original GAMIN trial. In GAMIN II, the investigators will evaluate 450 additional 1-59 month old children longitudinally for 6 months with a focus on stool collection and malaria status. Objectives: 1. To determine the effect of a single dose of azithromycin for children aged 8 days-59 months on malaria. The investigators hypothesize that a single dose of azithromycin will result in a reduced malaria status within the treatment group compared to the placebo group after a 14 day period within children ages 8 days-59 months. The study will be conducted in Nouna Town in northwestern Burkina Faso.

Eligibility Criteria

Inclusion Criteria

  • Between 8 days and 59 months old
  • Primary residence within catchment area of study site
  • Available for full 6 month study
  • No known allergy to macrolides/azalides
  • Appropriate written informed consent from at least one parent or guardian
  • Able to feed orally

Exclusion Criteria

  • 59 months
  • Primary residence outside catchment area of study site
  • Not available for full 6 month study
  • Known allergy to macrolides/azalides
  • No written informed consent from at least one parent or guardian
  • Unable to feed orally
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04315272). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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