MORDOR II Burkina Faso: Longitudinal Trial
NCT03676751 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 500
Last updated 2023-08-09
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.
Conditions
- Child Growth
- Diversity of Microbiome
- Child Mortality
- Resistance Bacterial
Interventions
- DRUG
-
Zithromax® for oral suspension is supplied in bottles containing azithromycin dehydrate powder equivalent to 1200mg per bottle and the following inactive ingredients: sucrose; tribasic anhydrous sodium phosphate; hydroxypropyl cellulose; xanthan gum; FD\&C Red #40; and flavoring including spray dried artificial cherry, crème de vanilla, and banana. After constitution, a 5mL suspension contains 200mg of azithromycin.
- DRUG
-
Oral suspension of placebo for azithromycin
Sponsors & Collaborators
-
Centre de Recherche en Sante de Nouna, Burkina Faso
collaborator OTHER_GOV -
Bill and Melinda Gates Foundation
collaborator OTHER -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Catherine Oldenburg, PhD · University of California, San Francisco
-
Ali Sie, MD, PhD · Centre de Recherce en Sante de Nouna
-
Tom Lietman, MD · University of California, San Francisco
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 8 Days
- Max Age
- 59 Months
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-10-10
- Primary Completion
- 2020-07-06
- Completion
- 2020-07-06
- FDA Drug
- Yes
Countries
- Burkina Faso
Study Locations
More Related Trials
-
Azithromycin for Child Survival in Niger: Programmatic Trial (AVENIR)
NCT05288023 ·Status: TERMINATED ·Phase: PHASE4
-
Improving Care Through Azithromycin Research for Infants in Africa
NCT04235816 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Antibiotic Resistance and Microbiome in Children Aged 6-59 Months in Nouna, Burkina Faso
NCT03187834 ·Status: COMPLETED ·Phase: PHASE4
-
Azithromycin to Prevent Post-discharge Morbidity and Mortality in Kenyan Children
NCT02414399 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
Azithromycin for Uncomplicated Severe Acute Malnutrition in Burkina Faso (Pilot)
NCT03568643 ·Status: COMPLETED ·Phase: PHASE3
-
Resiliency Through Azithromycin for Children (REACH), Côte d'Ivoire
NCT04617626 ·Status: COMPLETED ·Phase: NA
-
Azithromycin as Adjunctive Treatment for Uncomplicated Severe Acute Malnutrition
NCT06010719 ·Status: RECRUITING ·Phase: PHASE4
-
Antibiotics for Children With Severe Diarrhoea
NCT03130114 ·Status: COMPLETED ·Phase: PHASE3
-
Relative Efficacy of Two Regimens of Ante-helminthic Treatment
NCT00367627 ·Status: COMPLETED ·Phase: NA
-
REACH2: Implementation Research on Bi-Annual Mass Distribution of Azithromycin to Children 1-11 Months in Côte d'Ivoire
NCT05016895 ·Status: COMPLETED ·Phase: NA
-
Praziquantel in Children Under Age 4
NCT03640377 ·Status: COMPLETED ·Phase: PHASE2
-
A Pharmacokinetic and Safety Study of Moxidectin to Identify an Optimal Dose for Treatment of Children 4 to 11 Years
NCT03962062 ·Status: COMPLETED ·Phase: PHASE1
-
Novel Diagnostics and Probiotics to Improve Management of Paediatric Acute Gastroenteritis
NCT02025452 ·Status: COMPLETED ·Phase: PHASE4
-
Single Dose Azithromycin to Prevent Cholera in Children
NCT04326478 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study to Assess the Efficacy and Safety of Mebendazole for the Treatment of Helminth Infections in Pediatric Participants
NCT02034162 ·Status: COMPLETED ·Phase: PHASE3
-
Cluster RCT of Co-administration Azithromycin, Albendazole & Ivermectin
NCT03570814 ·Status: COMPLETED ·Phase: PHASE4
-
Mebendazole Study Against Hookworm Infections in Children and Adolescents in Ghana
NCT03261596 ·Status: WITHDRAWN ·Phase: PHASE4
-
Efficacy and Safety of a Multi-dose Regimen of Mebendazole Against Hookworm in Children
NCT03245398 ·Status: COMPLETED ·Phase: PHASE4
-
Safety of Co-administration of IDA and Azithromycin for NTDs ( ComboNTDs )
NCT03676140 ·Status: COMPLETED ·Phase: PHASE3
-
Better Options for Lymphatic Filariasis Treatment
NCT07159373 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Monitoring the Efficacy of Anthelmintics for the Treatment of Soil Transmitted Helminths P2
NCT01379326 ·Status: COMPLETED ·Phase: PHASE4
-
Cotrimoxazole Prophylaxis in Severely Malnourished Children
NCT00934492 ·Status: COMPLETED ·Phase: PHASE3
-
Package of Interventions After Recovering From Moderate Acute Malnutrition
NCT02351687 ·Status: COMPLETED ·Phase: NA
-
Validating Egg-based Diagnostics and Molecular Markers for the Spread of Anthelmintic Resistance
NCT03465488 ·Status: COMPLETED ·Phase: NA
-
Design and Clinical Evaluation of a School Meal With Deworming Properties
NCT02725255 ·Status: COMPLETED ·Phase: PHASE2/PHASE3