Additional Screening With Sensitives RDTs and Malaria

PHASE3CompletedINTERVENTIONAL
Enrollment

340

Participants

Timeline

Start Date

August 31, 2020

Primary Completion Date

August 31, 2021

Study Completion Date

December 31, 2021

Conditions
Plasmodium Falciparum MalariaMalaria Diagnosis
Interventions
DIAGNOSTIC_TEST

Additional screening using ultra sensitive RDTs

At each ANC visit, study nurses will perform an HS-RDT for participants in the intervention arm

DRUG

Dihydroartemisinin-piperaquin

All pregnant women with a positive HS-RDT will be treated with a full course of dihydroartemisinin-piperaquine (DP) over 3 days. The first dose of DP will be administered under direct observation at the antenatal care clinic (ANC) and the subsequent doses of the intervention in days 2 and 3 will be taken unsupervised at home

OTHER

Reminders

Before each scheduled ANC visit, reminders using SMS or phone call will be used. This is order to increase ANC attendance

Trial Locations (1)

218 CMS 11

Institut de Recherche en Sciences de la Santé/ Clinical Research Unit of Nanoro, Ouagadougou

All Listed Sponsors
collaborator

European and Developing Countries Clinical Trials Partnership (EDCTP)

OTHER_GOV

lead

Institut de Recherche en Sciences de la Sante, Burkina Faso

OTHER_GOV

NCT04147546 - Additional Screening With Sensitives RDTs and Malaria | Biotech Hunter | Biotech Hunter