Reducing the Burden of Malaria in HIV-uninfected Pregnant Women and Infants

NCT02163447 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2024-12-18

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Summary

This will be a double-blinded randomized controlled phase III trial of 300 HIV uninfected pregnant women and the children born to them. The study interventions will be divided into two phases. In the first phase, HIV uninfected women at 12-20 weeks gestation will be randomized in equal proportions to one of three intermittent preventive therapy in pregnancy (IPTp) treatment arms: 1) 3 doses of sulfadoxine-pyrimethamine (SP), 2) 3 doses of dihydroartemisinin-piperaquine (DP), or 3) monthly DP. All three interventions arms will have either SP or DP placebo to ensure adequate blinding is achieved. Follow-up for the pregnant women will end approximately 6 weeks after giving birth. In the second phase of the study, all children born to mothers enrolled in the study will be followed from birth until they reach 36 months of age. Children born to mothers randomized to receive 3 doses of SP during pregnancy will receive DP every 3 months between 2-24 months of age. Children born to mothers randomized to receive 3 doses of DP or monthly DP during pregnancy will receive either DP every 3 months or monthly DP between 2-24 months of age. To ensure adequate blinding, children who will receive DP every 3 months will be given DP placebo during the months they will not be taking DP. Children will then be followed an additional year between 24-36 months of age following the interventions. We will test the hypothesis that IPT with DP will significantly reduce the burden of malaria in pregnancy and infancy and improve the development of naturally acquired antimalarial immunity.

Conditions

Interventions

DRUG

Monthly dihydroartemisinin-piperaquine (DP) for adult women during pregnancy

DRUG

3 dose dihydroartemisinin-piperaquine (DP) for adult women during pregnancy

DRUG

3 dose sulfadoxine-pyrimethamine (SP) for adult women during pregnancy

DRUG

Monthly dihydroartemisinin-piperaquine (DP) for infants

DRUG

3-monthly dihydroartemisinin-piperaquine (DP) for infants

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH
  • Grant Dorsey, M.D, Ph.D.

    lead OTHER

Principal Investigators

  • Grant Dorsey, MD, PhD · University of California, San Francisco

  • Diane V Havlir, MD · University of California, San Francisco

  • Moses Kamya, MBChB, MMed, PhD · Makerere University; Infectious Diseases Research Collaboration

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-06-23
Primary Completion
2018-05-14
Completion
2018-05-14

Countries

  • Uganda

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02163447 on ClinicalTrials.gov