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Phase 4 N=450 Randomized Quadruple-blind Prevention

MORDOR II Burkina Faso: Longitudinal Trial

Child Growth · Diversity of Microbiome · Child Mortality · Resistance Bacterial

Enrolled (actual)
450
Serious AEs
0.0%
Results posted
Aug 2023
Primary outcome: Primary: Intestinal Microbial Diversity — 46.3; 49.5 index score

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
Jul 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Intestinal Microbial Diversity
46.3; 49.5
PRIMARY
Macrolide Resistance
98.89; 0.5
SECONDARY
Change in Weight Over Time
12.5; 12.6
SECONDARY
Change in Height Over Time
91.6; 91.3
SECONDARY
Number of Participants With Infantile Hypertrophic Pyloric Stenosis
0; 0
SECONDARY
Mortality
0; 0
SECONDARY
Malaria Status
14; 10
SECONDARY
Adverse Events
44; 42
SECONDARY
Genotypic Resistance
7547; 13077
SECONDARY
Inflammatory Marker Changes
SECONDARY
IgA-bound Bacteria From Small Intestine Changes
SECONDARY
Nutritional Status
14.3; 14.5
SECONDARY
Acute Modulation of the Gut Microbiome
SECONDARY
L-1 Norm Distance on Bacterial Reads (Intestinal)
32.98; 43.15
SECONDARY
L-2 Norm Distance on Bacterial Reads (Intestinal)
14.81; 20.46
SECONDARY
Changes in Normalized Reads for Campylobacter Species
1886.12; 549.48
SECONDARY
Resistome
3.98; 2.23

Summary

Globally, childhood mortality has shown a promising downward trend in recent years, however, many sub-Saharan countries still have relatively high child mortality rates. In previous studies within Niger, Tanzania, and Malawi, mass azithromycin treatment to children aged 1-59 months old effectively reduced all-cause childhood mortality. A similar study will be conducted in Burkina Faso to replicate the results of mass azithromycin treatment. The investigators propose an individually randomized placebo-controlled trial alongside the MORDOR II Burkina Faso trial 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. Many questions surround the mechanism behind azithromycin's effect on reducing childhood mortality. Further questions exist regarding antibiotic resistance and how mass antibiotic administration can impact intestinal microflora. The goal of this study is to demonstrate the changes in the gut microbiome after antibiotic administration and to measure the growth of children after receiving a single dose of azithromycin. Additionally we will measure resistance markers, inflammatory markers, and IgA-bound bacteria. We hypothesize that a single dose of azithromycin will lead to a significant increase in child growth and that the gut microbiome will be significantly different in children who received azithromycin compared to those who received placebo. Objectives: 1. . To determine the effect of a single dose of azithromycin for children aged 8 days-59 months on longitudinal changes in the intestinal microbiome over a 6-month period. We hypothesize that a single dose of azithromycin will result in a significant difference in the intestinal microbiome within the treatment group compared to the placebo group after a 6-month period within children ages 8 days-59 months. 2. . To determine the effect of a single dose of azithromycin for children aged 8 days-59 months on child growth over a 6-month period. We hypothesize that a single dose of azithromycin will increase child growth over a 6-month period in children aged 8 days-59 months. 3. . To determine the effect of a single dose of azithromycin for children aged 8 days to 59 months on the presence of macrolide genetic resistance determinants within the first two weeks post-treatment. The investigators hypothesize that a single dose of azithromycin will increase the presence of macrolide resistance determinants over a 2 week period in children aged 8 days to 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 (NCT03676751). 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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