Skip to content

Malaria Prevention in pregnancy in Tanzania

Effectiveness of the combination of dihydroartemisinin and piperaquine for prevention of falciparum malaria during pregnancy in Tanzania

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201612001901313
Enrollment
1000
Registered
2016-12-02
Start date
2017-01-02
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malaria

Interventions

Intermittent preventive treatment with Dihydroartemisinin/piperaquine
Intermittent prevetive treatment with Sulfadoxine/Pyrimethamine
Daily co-trimoxazole alone given to HIV infected pregnant women
IPTDihydroartemisinin and piperaquine added to daily cotrimoxazole among HIV infected pregnant women

Sponsors

MUHAS
Lead Sponsor
Sida-MUHAS
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: i. Viable pregnancy assessed by UPT ii. Gestational age 16 to 32 weeks (inclusive) determined by fundal height iii. No prior history of IPTp use for current pregnancy iv. Willing to participate and complete the study schedule v. Willing to sign or thumb print informed consent vi. Resident of study area and intending to stay in the area for the duration of the follow-up vii. Willing to deliver at the health facility

Exclusion criteria

Exclusion criteria: i. Residence outside study area or planning to move out in the 12 months following enrolment ii. High risk pregnancy, including any pre-existing illness likely to cause complication of pregnancy (hypertension, diabetes, asthma, epilepsy, renal disease, liver disease, fistula repair, leg or spine deformity) iii. Severe anemia requiring blood transfusion (Hb ¿ 7.0 g/dL) at enrolment iv. Known allergy or previous adverse reaction to any of the study drugs v. Unable to give informed consent (for example due to mental disability) vi. Previous inclusion in the same study

Design outcomes

Primary

MeasureTime frame
Active or recent placental malaria

Secondary

MeasureTime frame
¿ Incidence of malaria infection and clinical malaria during pregnancy, defined as fever or recent history of fever in the presence of malaria parasites; ¿ Prevalence of adverse newborn morbidity at birth, defined as a composite of either preterm delivery (<37 weeks¿ gestation), low birth weight (<2500 g), and, anemia (hemoglobin<11 g/dL) during pregnancy or at delivery

Countries

Tanzania

Contacts

Public ContactMwelecele Malcela

Chairperson Medical Research Committee/National Institute for Medical Researches

headquarters@nimr.or.tz+255222121400

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026