Improving Neonatal Health Through Rapid Malaria Testing in Early Pregnancy With High-Sensitivity Diagnostics (INTREPiD)
Malaria,Falciparum, Malaria in Pregnancy, Malaria in Childbirth
About this trial
This is an interventional screening trial for Malaria,Falciparum
Eligibility Criteria
Inclusion Criteria: Aged between 16 years and 40 years (inclusive) Viable singleton pregnancy with gestational age estimated less than 13 6/7 weeks (inclusive) by ultrasound HIV-uninfected Willing to participate in the study schedule Planning to remain in the study area for the duration of pregnancy and 1 month after delivery Willing to deliver in a study-affiliated health facility Exclusion Criteria: High risk pregnancy that requires referral for specialized care by local guidelines Active medical problem at the time of screening requiring higher level care Antimalarial receipt in the 2 weeks prior to screening Past allergy to Artemether or Lumefantrine or another condition that prohibits the receipt of either drug Current participation in another clinical research study
Sites / Locations
- Kinshasa School of Public Health
- Moi University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
HS-RDT screening/AL treatment
Usual antenatal care
Pregnant women will be screened with a malaria HS-RDT and, if positive, treated with artemether-lumefantrine
Pregnant women will receive usual antenatal care