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Malaria in Pregnancy: Nutrition and Immunologic Effects

Not Applicable
Completed
Conditions
Malaria
Low Birth Weight
Perinatal Mortality
Anemia
Interventions
Other: Placebo
Dietary Supplement: Vitamin A
Dietary Supplement: Zinc
Registration Number
NCT01115478
Lead Sponsor
Harvard School of Public Health (HSPH)
Brief Summary

The purpose of this study is to determine the efficacy of zinc and/or vitamin A supplementation in reducing the risk of placental malaria and its associated adverse pregnancy outcomes.

Detailed Description

Malaria accounts for a major proportion of the disease burden in Tanzania with 14 to 18 million new malaria cases being reported each year resulting in 100,000-125,000 deaths. Malaria results in impaired productivity for those between 15-55 years and lost learning opportunities in the 5-25 year age group. Dar es Salaam is characterized as an area with endemic and perennial malaria, with transmission occurring during the entire year. P. falciparum accounts for more than 95% of malaria infections. A number of interventions have contributed to reducing the burden of the disease in some settings in Tanzania and beyond, including vector control measures, bed nets, and prophylaxis and treatment of malaria. However, malaria remains a serious problem among pregnant women and children. We will examine the efficacy of micronutrient supplements as a means of enhancing immune response to malaria in pregnancy and reducing the risks of associated adverse clinical outcomes. If successful, such a low-cost intervention would be added to the armamentarium against this disease.

NOTE: The time frames listed for the maternal malaria and hemoglobin outcomes were updated on 4/22/15. This record initially indicated that maternal malaria anemia and hemoglobin would be measured at several specific time points throughout the study. Instead, maternal malaria was measured throughout pregnancy and hemoglobin was measured only at delivery. Due to an oversight, we did not update this record when this protocol change took effect at the start of the study.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
2500
Inclusion Criteria
  • Primigravida or secundigravidae
  • At or before 13 weeks of gestation
  • HIV-negative
  • Intend to stay in Dar es Salaam until delivery and for at least 6 weeks thereafter
Exclusion Criteria
  • Not primigravida or secundigravidae
  • After 13 weeks of gestation
  • HIV-positive
  • Do not intend to stay in Dar es Salaam until delivery and for at least 6 weeks thereafter

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Vitamin A + ZincZinc-
PlaceboPlacebo-
Vitamin AVitamin A-
ZincZinc-
Vitamin A + ZincVitamin A-
Primary Outcome Measures
NameTimeMethod
Incidence of placental malariaDelivery

Placental infection status will be categorized as infected if there are asexual parasites in the placenta blood; not infected if the placental blood smear is negative; or status unknown if no placental smear is available.

Low birth weightDelivery

Low birth weight will be defined as birth weight less than 2500 grams.

Secondary Outcome Measures
NameTimeMethod
Maternal anemiaDelivery

Anemia is defined as hemoglobin less than 11 g/dl. Severe anemia is less than 8.5 g/dl.

Perinatal deathat or after 28 weeks of gestation and in the first 7 days of life
Maternal malariaDuring pregnancy

Maternal malaria will be defined as fever within the last 72 hours with any parasitemia on a peripheral blood smear.

Trial Locations

Locations (1)

Muhimbili University of Health And Allied Sciences

🇹🇿

Dar es Salaam, Tanzania

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