search
Back to results

A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children (SMCAZ)

Primary Purpose

Malaria, Respiratory Infections

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Sulphadoxine-Pyrimethamine+ Amodiaquine+ Azithromycin
Sulphadoxine-pyrimethamine + amodiaquine + placebo azithromycin
Sponsored by
London School of Hygiene and Tropical Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malaria

Eligibility Criteria

3 Months - 59 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Children of either sex aged 3-59 months of age at the start of each period of drug administration
  • parental consent is obtained.

Exclusion Criteria:

  • a severe, chronic illness,
  • a known allergy to one of the study drugs.
  • HIV+ children on cotrimoxazole prophylaxis

Sites / Locations

  • Hounde district Hospital
  • Bougouni Koulikoro District hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Seasonal malaria chemoprevention

seasonal malaria chemoprevention plus AZ

Arm Description

Sulphadoxine-Pyrimethamine Amodiaquine Placebo Azithromycin

Sulphadoxine-Pyrimethamine+ Amodiaquine + Azithromycin 4 rounds during malaria transmission season

Outcomes

Primary Outcome Measures

severe morbidity and mortality
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

macrolide resistant pneumococci carriage

Full Information

First Posted
July 17, 2014
Last Updated
March 6, 2018
Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
Malaria Research and Training Center, Bamako, Mali, Institut de Recherche en Sciences de la Sante, Burkina Faso
search

1. Study Identification

Unique Protocol Identification Number
NCT02211729
Brief Title
A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children
Acronym
SMCAZ
Official Title
A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
May 2014 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
Malaria Research and Training Center, Bamako, Mali, Institut de Recherche en Sciences de la Sante, Burkina Faso

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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: incidence of the primary endpoint during the whole study period attendance at a study health centre with a nonmalaria febrile illness attendance at a study health centre with malaria, the prevalence of moderate anaemia at the end of each malaria transmission season, nutritional status at the end of each malaria transmission season, prevalence of nasopharyngeal carriage with pneumococci and macrolide resistant pneumococci before and at the end of each malaria transmissions season, prevalence of resistance markers to SP at the end of the study, Sample size: 19,200 children (9600 in each country) will be enrolled.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Respiratory Infections

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
22090 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Seasonal malaria chemoprevention
Arm Type
Active Comparator
Arm Description
Sulphadoxine-Pyrimethamine Amodiaquine Placebo Azithromycin
Arm Title
seasonal malaria chemoprevention plus AZ
Arm Type
Experimental
Arm Description
Sulphadoxine-Pyrimethamine+ Amodiaquine + Azithromycin 4 rounds during malaria transmission season
Intervention Type
Drug
Intervention Name(s)
Sulphadoxine-Pyrimethamine+ Amodiaquine+ Azithromycin
Intervention Description
Sulphadoxine-Pyrimethamine+ Amodiaquine+ Azithromycin 4 rounds during malaria transmission season
Intervention Type
Drug
Intervention Name(s)
Sulphadoxine-pyrimethamine + amodiaquine + placebo azithromycin
Intervention Description
Sulphadoxine-pyrimethamine + amodiaquine + placebo azithromycin 4 rounds during malaria transmission season
Primary Outcome Measure Information:
Title
severe morbidity and mortality
Description
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.
Time Frame
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)
Secondary Outcome Measure Information:
Title
macrolide resistant pneumococci carriage
Time Frame
before administration of first dose of SMC and at the end of malaria transmission season in year 1, 2 and 3,
Other Pre-specified Outcome Measures:
Title
out patient attendance for non malaria febrile illness
Description
(b) attendance at a study health centre with a febrile illness that is not due to malaria (including acute respiratory infections and diarrhoea),
Time Frame
from enrolment until the end of malaria transmission season in year 3
Title
OPD attendance for malaria
Description
(c) attendance at a study health centre with RDT or microscopically proven malaria,
Time Frame
from enrollment until the end of malaria transmission season in year 3
Title
moderate anaemia
Description
(d) the prevalence of moderate anaemia (Hb <8 g/dL) at the end of each malaria transmission season,
Time Frame
at the end of each malaria transmission season in year 1, 2, and 3
Title
nutritional status
Description
(e) nutritional status at the end of each malaria transmission season,
Time Frame
at the end of malaria transmission season in year 1, 2 and 3
Title
nasopharyngeal carriage
Description
(f) the prevalence of nasopharyngeal carriage with pneumococci before and at the end of each malaria transmissions season,
Time Frame
before the administration of first dose of SMC and at the end of malaria transmission season in year 1, 2, and 3
Title
SP resistance markers
Description
(h) the prevalence of resistance markers to SP in children with Plasmodium falciparum malaria at the end of the study,
Time Frame
at the end of the malaria transmission season in year 3
Title
adverse events
Description
solicited adverse events 7 days after administration of SMC+AZ after each round in the year one of the study
Time Frame
7 days after administration of SMC in rounds 1, 2, 3 and 4 in year one

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children of either sex aged 3-59 months of age at the start of each period of drug administration parental consent is obtained. Exclusion Criteria: a severe, chronic illness, a known allergy to one of the study drugs. HIV+ children on cotrimoxazole prophylaxis
Facility Information:
Facility Name
Hounde district Hospital
City
Hounde
Country
Burkina Faso
Facility Name
Bougouni Koulikoro District hospital
City
Bougouni
Country
Mali

12. IPD Sharing Statement

Citations:
PubMed Identifier
34644317
Citation
Hema-Ouangraoua S, Tranchot-Diallo J, Zongo I, Kabore NF, Nikiema F, Yerbanga RS, Tinto H, Chandramohan D, Ouedraogo GA, Greenwood B, Ouedraogo JB. Impact of mass administration of azithromycin as a preventive treatment on the prevalence and resistance of nasopharyngeal carriage of Staphylococcus aureus. PLoS One. 2021 Oct 13;16(10):e0257190. doi: 10.1371/journal.pone.0257190. eCollection 2021.
Results Reference
derived
PubMed Identifier
32822362
Citation
Cairns ME, Sagara I, Zongo I, Kuepfer I, Thera I, Nikiema F, Diarra M, Yerbanga SR, Barry A, Tapily A, Coumare S, Milligan P, Tinto H, Ouedraogo JB, Chandramohan D, Greenwood B, Djimde A, Dicko A. Evaluation of seasonal malaria chemoprevention in two areas of intense seasonal malaria transmission: Secondary analysis of a household-randomised, placebo-controlled trial in Hounde District, Burkina Faso and Bougouni District, Mali. PLoS Med. 2020 Aug 21;17(8):e1003214. doi: 10.1371/journal.pmed.1003214. eCollection 2020 Aug.
Results Reference
derived
PubMed Identifier
30699301
Citation
Chandramohan D, Dicko A, Zongo I, Sagara I, Cairns M, Kuepfer I, Diarra M, Barry A, Tapily A, Nikiema F, Yerbanga S, Coumare S, Thera I, Traore A, Milligan P, Tinto H, Doumbo O, Ouedraogo JB, Greenwood B. Effect of Adding Azithromycin to Seasonal Malaria Chemoprevention. N Engl J Med. 2019 Jun 6;380(23):2197-2206. doi: 10.1056/NEJMoa1811400. Epub 2019 Jan 30.
Results Reference
derived

Learn more about this trial

A Trial of Seasonal Malaria Chemoprevention Plus Azithromycin in African Children

We'll reach out to this number within 24 hrs