Post-discharge Malaria Chemoprevention(PMC) Study

PHASE3CompletedINTERVENTIONAL
Enrollment

1,049

Participants

Timeline

Start Date

May 20, 2016

Primary Completion Date

October 24, 2018

Study Completion Date

December 12, 2018

Conditions
MalariaSevere Anemia
Interventions
DRUG

dihydroartemisinin-piperaquine

Children in both arms will receive standard in-hospital care for severe anaemia (blood transfusion, often combined with quinine or artesunate IV/IM). All children will then receive a 3-day course of AL (whether they initially had malaria or not), which will be started in-hospital as soon as they are able to take oral medication, and will be completed at home after discharge. At 2 weeks after enrolment surviving children will be randomized to receive either a standard 3-day courses of dihydroartemisinin-piperaquine (Eurartesim®, Sigma Tau, Italy) or an identical placebo regimen at 2, 6 and 10 weeks after enrolment.

DRUG

dihydroartemisinin-piperaquine placebo

Children will receive standard in-hospital care for severe anaemia (blood transfusion, often combined with quinine or artesunate IV/IM). All children will then receive a 3-day course of AL (whether they initially had malaria or not), which will be started in-hospital as soon as they are able to take oral medication, and will be completed at home after discharge. At 2 weeks after enrolment surviving children will be randomized to receive either a standard 3-day courses of dihydroartemisinin-piperaquine (Eurartesim®, Sigma Tau, Italy) or an identical placebo regimen at 2, 6 and 10 weeks after enrolment.

Trial Locations (9)

40100

Homa Bay County Referral Hospital, Homa Bay

Siaya County Referral Hospital, Siaya

40400

Migori County Referral Hospital, Migori

Unknown

Jaramogi Oginga Odinga Teaching and Referral Hospital, Kisumu

Hoima Regional Referral Hospital, Hoima

Jinja Regional Referral Hospital, Jinja

Kamuli Mission Hospital, Kamuli

Masaka Regional Referral Hospital, Masaka

Mubende Regional Referral Hospital:, Mubende

Sponsors
All Listed Sponsors
collaborator

The Research Council of Norway

OTHER

collaborator

Kenya Medical Research Institute

OTHER

collaborator

Makerere University

OTHER

lead

Liverpool School of Tropical Medicine

OTHER