CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 347 enrolled
Drug / intervention
Azithromycin +1 moredrug
Likely dose
Not stated in record
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Search/NCT02426112
NCT02426112Phase 3Completed

Bronchopulmonary Function in Response to Azithromycin Treatment for Chronic Lung Disease in HIV-infected Children

London School of Hygiene and Tropical Medicine·interventional·Posted Apr 24, 2015·Updated Oct 9, 2019

In Brief

A Phase 3 clinical trial evaluating Azithromycin and Placebo for Chronic Lung Disease and HIV Infection. Completed, enrolled 347 participants across 2 sites in 2 countries.

Detailed Summary

Chronic pulmonary disease (CLD) is the most common manifestation of HIV/AIDS among children, accounting for more than 50% of HIV-associated mortality. Recently, a novel form of CLD, affecting more than 30% of African HIV-infected older children was described by Ferrand et al in Zimbabwe, high-resolution CT scanning findings showed predominantly small airways disease consistent with constrictive obliterative bronchiolitis (OB). . Azithromycin has anti-inflammatory activity and treatment of CLD with this agent may lead to suppression of generalized immune activation. This specific aims of this project are to: 1. Primary objective: To investigate whether adjuvant treatment with azithromycin results in improvement in lung function in HIV-infected children with chronic lung disease, who are stable on antiretroviral therapy. 2. Secondary objectives: 1. To investigate the intervention effect on mortality, exacerbations of lung disease, quality of life, morbidity. 2. To investigate adverse events related to azithromycin treatment In total, 400 children aged 6-16 years, living with HIV and diagnosed with CLD will be enrolled at Harare Children´s Hospital in Harare (Zimbabwe) and Queen Elizabeth Central Hospital in Blantyre (Malawi). These will receive weekly treatment with azithromycin or placebo during 12 months. Another 100 children (50 per site) living with HIV but with no CLD will be enrolled as a comparison group for laboratory sub-studies. Lung function will be assess using spirometry and the Forced expiratory volume in the first minute (FEV1) will be the primary outcome. The mean change in FEV1 z-score levels will be compared between trial arms after 12 months of initiation of azithromycin treatment.

Study Details

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedApr 24, 2015
Enrollment StartJun 1, 2016
Primary CompletionSep 1, 2018
Study CompletionAug 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 11.2 years ago

Interventions

Azithromycindrug

Placebodrug