Phase 4
N=450
MORDOR II Burkina Faso: Longitudinal Trial
Child Growth · Diversity of Microbiome · Child Mortality · Resistance Bacterial
Bottom Line
View on ClinicalTrials.gov: NCT03676751 ↗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
| Outcome | Result | p-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
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.