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Clinical Trials/NCT00680732
NCT00680732
Completed
Phase 4

Prevention of Intrauterine Growth Retardation in Hounde District, Burkina Faso: the Malaria Component

Institute of Tropical Medicine, Belgium1 site in 1 country1,370 target enrollmentJune 2003

Overview

Phase
Phase 4
Intervention
Multiple micronutrients supplements (MMS)
Conditions
Malaria
Sponsor
Institute of Tropical Medicine, Belgium
Enrollment
1370
Locations
1
Primary Endpoint
Efficacy of standard antimalarial treatment in preventing clinical malaria in pregnant women under weekly chemoprophylaxis or intermittent treatment.
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Our objective was to investigate the importance of malaria infection/disease during pregnancy and more particularly during the first trimester; we also looked at the maternal-foetal interactions and their influence on the subsequent child's response to malaria infections during the first year of life. This study was carried out !in the same population recruited for the IUGR study (NCT00642408).

Detailed Description

A research project aiming at investigating the impact of multivitamin-mineral supplementation (MMS) during pregnancy on intra-uterin growth retardation was carried out in the Hounde district, an area not far from the Centre Muraz located in Bobo Dioulasso, and where malaria is endemic. Malaria during pregnancy increases the risk of low birth weight, infant mortality and morbidity during the first year of life by inducing growth retardation, prematurity and infant anaemia. The administration of an antimalarial drug during pregnancy has a beneficial effect on the mother and child's health by preventing malaria infection and its consequences. However, most studies have been carried out during the second or third trimester of pregnancy: the effect of malaria infection during the first trimester on the mother's and child's health is unknown. It has been reported that even one single infection may have a significant impact on the outcome of pregnancy: if it is true, then early chemoprophylaxis may have an additional advantage. An alternative approach is the administration of intermittent presumptive treatment, which may achieve equal efficacy to continuos chemoprophylaxis; however, no studies compared effective weekly malaria chemoprophylaxis with effective intermittent presumptive treatment. Moreover, the incidence of malaria clinical episodes during SP intermittent preventive treatment has never been investigated. Therefore, this open label, factorial study was carried out in the same women recruited for the IUGR nutritional study (NCT00642408). Women receiving multiple micronutrients supplements (MMS) or dietary supplements (IFA) were further randomised in 2 groups: CQ weekly chemoprophylaxis or SP intermittent preventive treatment. The administration of treatment was directly observed.

Registry
clinicaltrials.gov
Start Date
June 2003
End Date
October 2006
Last Updated
15 years ago
Study Type
Interventional
Study Design
Factorial
Sex
Female

Investigators

Sponsor
Institute of Tropical Medicine, Belgium

Eligibility Criteria

Inclusion Criteria

  • 15 to 44 years
  • living in the study area

Exclusion Criteria

  • planning to move outside the district within two years
  • regularly using a contraceptive methods
  • already pregnant at the start of the trial

Arms & Interventions

A1

Multiple micronutrients supplements (MMS) and weekly chloroquine (CQ)

Intervention: Multiple micronutrients supplements (MMS)

A1

Multiple micronutrients supplements (MMS) and weekly chloroquine (CQ)

Intervention: Chloroquine (CQ)

A2

Multiple micronutrients supplements (MMS) and intermittent suplphadoxyne-pyrimethamine (SP)

Intervention: Multiple micronutrients supplements (MMS)

A2

Multiple micronutrients supplements (MMS) and intermittent suplphadoxyne-pyrimethamine (SP)

Intervention: Sulphadoxyne-pyrimethamine (SP)

B1

Iron and folic acid (IFA) and weekly chloroquine (CQ)

Intervention: Iron and folic acid (IFA)

B1

Iron and folic acid (IFA) and weekly chloroquine (CQ)

Intervention: Chloroquine (CQ)

B2

Iron and folic acid (IFA) and intermittent sulphadoxyne-pyrimethamine (SP)

Intervention: Iron and folic acid (IFA)

B2

Iron and folic acid (IFA) and intermittent sulphadoxyne-pyrimethamine (SP)

Intervention: Sulphadoxyne-pyrimethamine (SP)

Outcomes

Primary Outcomes

Efficacy of standard antimalarial treatment in preventing clinical malaria in pregnant women under weekly chemoprophylaxis or intermittent treatment.

Time Frame: Up to delivery

Secondary Outcomes

  • To determine if the occurrence of malaria during pregnancy influences the incidence of clinical malaria in infants during their first year of life.(Up to one year after delivery)
  • To determine the burden of clinical malaria during pregnancy and its consequences on maternal anaemia, new birth weight and foetal anaemia.(Up to delivery)
  • Effect of standard antimalarial treatment on the selection of resistant parasites in pregnant women under weekly chemoprophylaxis or intermittent treatment.(Up to one year after delivery)

Study Sites (1)

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