CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 21,832 enrolled
Drug / intervention
Azithromycin +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03682653
NCT03682653Phase 4Completed

Neonates and Azithromycin, an Innovation in the Treatment of Children in Burkina Faso

University of California, San Francisco·interventional·Posted Sep 24, 2018·Updated Jun 27, 2023

In Brief

A Phase 4 clinical trial evaluating Azithromycin and Placebo for Childhood Mortality. Completed, enrolled 21,832 participants across 1 site.

Detailed Summary

Although under-5 mortality rates are declining globally, neonatal mortality remains persistently high in many regions of sub-Saharan Africa. Mass azithromycin distribution to children aged 1-59 months has been shown to reduce childhood mortality in Niger, Tanzania, and Malawi. This study did not evaluate the effect of azithromycin administered during the neonatal period. Observational evidence from high income countries has suggested that macrolides, including erythromycin and azithromycin, may be associated with increased risk of development of infantile hypertrophic pyloric stenosis (IHPS). However, these studies are limited by confounding by indication, as infants only receive antibiotics when they are ill. The investigators proposed an individually randomized trial of azithromycin versus placebo to establish the efficacy and safety of administration of a dose of azithromycin during the neonatal period. The long-term goal is generate evidence that can be used by neonatal and child survival programs related to the use of azithromycin in the youngest children who have the highest risk of mortality. The investigators hypothesize that a single dose of azithromycin administered in the neonatal period will lead to significantly reduced risk of mortality and that this dose will be safe. Objectives 1. Establish the efficacy of a single dose of azithromycin administered during the neonatal period compared to placebo in infants 8 to 27 days of life for reduction in all-cause mortality. 2. Establish the safety of a single dose of azithromycin administered during the neonatal period. This study will be conducted in several regions of Burkina Faso, including peri-urban areas of Ouagadougou and Nouna town, and rural areas that are within 4 hours' drive of a pediatric facility with capacity for performing pyloromyotomy

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBurkina Faso

Timeline

Phase 4CompletedFinished
20192020202120222023202420252026
First PostedSep 24, 2018
Enrollment StartApr 11, 2019
Primary CompletionMay 1, 2022
Study CompletionDec 31, 2022
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 7.8 years ago

Interventions

Azithromycindrug

a single dose of Azithromycin will be administered to infants between their 8-27th days of life

Placebodrug

a single dose of Placebo will be administered to infants between their 8-27th days of life