Clinical Trials Directory

Trials / Completed

CompletedNCT02211729

A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
22,090 (actual)
Sponsor
London School of Hygiene and Tropical Medicine · Academic / Other
Sex
All
Age
3 Months – 59 Months
Healthy volunteers
Accepted

Summary

The primary objective of this study is to determine whether addition of azithromycin (AZ) to Seasonal Malaria Chemoprevention (SMC) using sulphadoxine/pyrimethamine (SP) +amodiaquine (AQ) will provide an additional reduction in deaths and severe illness in young African children. The secondary objectives include an assessment of the safety and cost-effectiveness of the addition of AZ to SMC with SP+AQ. This a double blind, randomised, placebo controlled trial. The unit of randomisation will be the household. Children aged 3 - 59 months will be randomised to receive four cycles of either SP+AQ+AZ or SP+AQ+ placebo at monthly intervals during the peak malaria transmission season. Study Sites: Hounde district in Burkina Faso and in Bougouni district, Mali. Children of 3-59 months of age at the start of each period of drug administration will be eligible for inclusion in the trial provided that parental consent is obtained. Children with a severe, chronic illness or known allergy to one of the study drugs will be excluded. Primary endpoint: Incidence of the combination of death or hospital admission for at least 24 hours, not due to trauma or elective surgery during the intervention period Secondary endpoints: 1. incidence of the primary endpoint during the whole study period 2. attendance at a study health centre with a nonmalaria febrile illness 3. attendance at a study health centre with malaria, 4. the prevalence of moderate anaemia at the end of each malaria transmission season, 5. nutritional status at the end of each malaria transmission season, 6. prevalence of nasopharyngeal carriage with pneumococci and macrolide resistant pneumococci before and at the end of each malaria transmissions season, 7. prevalence of resistance markers to SP at the end of the study, Sample size: 19,200 children (9600 in each country) will be enrolled.

Conditions

Interventions

TypeNameDescription
DRUGSulphadoxine-Pyrimethamine+ Amodiaquine+ AzithromycinSulphadoxine-Pyrimethamine+ Amodiaquine+ Azithromycin 4 rounds during malaria transmission season
DRUGSulphadoxine-pyrimethamine + amodiaquine + placebo azithromycinSulphadoxine-pyrimethamine + amodiaquine + placebo azithromycin 4 rounds during malaria transmission season

Timeline

Start date
2014-05-01
Primary completion
2017-12-31
Completion
2017-12-31
First posted
2014-08-07
Last updated
2018-03-07

Locations

2 sites across 2 countries: Burkina Faso, Mali

Source: ClinicalTrials.gov record NCT02211729. Inclusion in this directory is not an endorsement.