A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children
- Conditions
- MalariaRespiratory Infections
- Interventions
- Registration Number
- NCT02211729
- Lead Sponsor
- London School of Hygiene and Tropical Medicine
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 22090
- Children of either sex aged 3-59 months of age at the start of each period of drug administration
- parental consent is obtained.
- a severe, chronic illness,
- a known allergy to one of the study drugs.
- HIV+ children on cotrimoxazole prophylaxis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description seasonal malaria chemoprevention plus AZ Sulphadoxine-Pyrimethamine+ Amodiaquine+ Azithromycin Sulphadoxine-Pyrimethamine+ Amodiaquine + Azithromycin 4 rounds during malaria transmission season Seasonal malaria chemoprevention Sulphadoxine-pyrimethamine + amodiaquine + placebo azithromycin Sulphadoxine-Pyrimethamine Amodiaquine Placebo Azithromycin
- Primary Outcome Measures
Name Time Method severe morbidity and mortality from the time of enrolment upto the end of malaria transmission in year 3 ( the person time at risk will be restricted to three malaria transmission seasons) 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 Outcome Measures
Name Time Method macrolide resistant pneumococci carriage before administration of first dose of SMC and at the end of malaria transmission season in year 1, 2 and 3,
Trial Locations
- Locations (2)
Hounde district Hospital
🇧🇫Hounde, Burkina Faso
Bougouni Koulikoro District hospital
🇲🇱Bougouni, Mali