Daily Co-trimoxazole Prophylaxis to Prevent Malaria in Pregnancy
Information source: Institute of Tropical Medicine, Belgium
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Malaria in Pregnancy
Intervention: Cotrimoxazole (Drug); Sulfadoxine-pyrimethamine (Drug)
Phase: Phase 3
Status: Terminated
Sponsored by: Institute of Tropical Medicine, Belgium Official(s) and/or principal investigator(s): Christine Manyando, MD, Principal Investigator, Affiliation: Tropical Diseases Research Centre Jean-Pierre Van geertruyden, MD PhD, Study Director, Affiliation: Institute of Tropical medicine
Summary
Malaria is a major contributor of disease burden in Sub-Saharan Africa, and pregnant women
and children are the most vulnerable population. Malaria in pregnancy increases the risks of
abortion, prematurity, maternal anaemia, low birth weight (LBW), perinatal, neonatal and
infant mortality. For prevention and control of malaria in pregnancy, Intermittent
Preventive Treatment (IPT), insecticide treated nets (ITNs) and case management for malaria
and anemia are recommended.
HIV infection in pregnancy increases the risk of malaria, LBW, post-natal mortality and also
of anaemia. In pregnant women, HIV infection decreases the efficacy of IPT with the medicine
sulfadoxine-pyrimethamine (SP), which is the only treatment with proven efficacy and safety
in IPT and is recommended by the World Health Organization (WHO). Unfortunately, there is a
documented increase of resistance to SP, so cotrimoxazole (CTX) could be an alternative:
many studies in Zambia and Uganda demonstrated that it reduces mortality and morbidity in
HIV infected persons, and CTX prophylaxis significantly improves birth outcomes in
immuno-suppressed HIV women. Unfortunately, there is not yet information on its
effectiveness for preventing placental malaria infection, maternal anaemia and LBW. Thus in
this study, we aim to establish the safety and efficacy of daily CTX in preventing malaria
infection during pregnancy and its consequences, both in HIV infected and non-infected
pregnant women. This information is urgently needed to assist to issue guidelines on IPT in
pregnancy.
Clinical Details
Official title: The Role of Daily Co-trimoxazole Prophylaxis For Prevention of Malaria And Its Effects in Pregnancy
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Primary outcome: To test the hypothesis that co-trimoxazole prophylaxis is not inferior to SP intermittent preventive treatment in preventing placental malaria.
Secondary outcome: To evaluate efficacy of CTX prophylaxis in preventing malaria peripheral parasitaemia.To evaluate efficacy of CTX prophylaxis in preventing perinatal mortality and in improving birth weight To establish the safety of CTX prophylaxis on the offspring by measuring the gestational age at delivery and birth weight. To compare the efficacy profile of CTX prophylaxis to that of SP intermittent preventive treatment. To compare the safety profile of CTX prophylaxis to that of SP intermittent preventive treatment. Spontaneous abortion Pre-term delivery Neonatal mortality Maternal mortality Major and minor birth defects
Detailed description:
Malaria is a major contributor of disease burden in Sub-Saharan Africa, with pregnant women
and children being the most vulnerable population. P. falciparum infection in pregnancy
leads to parasite sequestration in placental vascular space, with increased risks of
abortion, stillbirth, prematurity, intrauterine growth retardation, maternal anaemia, low
birth weight (LBW), perinatal, neonatal and infant mortality. In low transmission areas,
malaria can evolve towards severe disease with high risk of mortality. In endemic areas, it
is still associated with maternal anaemia, LBW and stillbirth. For prevention and control of
malaria in pregnancy, WHO recommends Intermittent Preventive Treatment (IPT), insecticide
treated nets (ITNs) and case management for malaria and anemia.
HIV in pregnancy increases the risk of malaria, LBW, post-natal mortality and also anaemia,
suggesting a synergistic interaction between HIV and malaria.
In pregnant women, HIV-1 infection decreases the efficacy of
sulfadoxine-pyrimethamine(SP)IPT, although 2 or more doses in 2nd and 3rd trimesters still
reduce peripheral parasitaemia, placental infections and maternal anaemia.
To date, SP is the only treatment with data on efficacy and safety in IPT: WHO recommends at
least 2 doses after the first trimester. But there is a documented increase in SP
resistance, so cotrimoxazole (CTX) could be an alternative: many studies in Zambia and
Uganda demonstrated that it reduces mortality and morbidity in HIV infected individuals, and
CTX prophylaxis significantly improves birth outcomes in women with CD4 count <200.
Concurrent administration of SP and CTX has been associated with increased incidence of
severe adverse reactions in HIV-infected patient.
WHO has promoted CTX as alternative to SP for IPT in immuno-compromised HIV-infected
pregnant women. Unfortunately, there is no information on effectiveness of daily CTX for
preventing placental malaria infection, maternal anaemia and LBW. In the past, CTX has been
used to treat malaria in children and daily use of CTX by non-pregnant HIV-infected adults
has been associated with a 70% reductions of the incidence of clinical malaria.
In this study, we will target both HIV infected and non-infected pregnant women with CD4≥
200/µL, with the aim to establish the safety and efficacy of daily CTX in preventing malaria
infection during pregnancy and its consequences, by assuming that CTX is not inferior to SP
in reducing placental parasitaemia: such information is urgently needed to assist to issue
guidelines on IPT in pregnant women.
Eligibility
Minimum age: N/A.
Maximum age: N/A.
Gender(s): Female.
Criteria:
Inclusion Criteria:
- Confirmed pregnancy (through palpable fundus and/ or positive pregnancy test)
- Gestational age between 16 and 28 weeks.
- Informed consent by patient (or parent/ guardian if patient is less than 18 years of
age)
- No symptoms consistent with malaria
- Willingness to deliver at the health facility
- Willingness to adhere to all requirements of the study (including HIV-1 testing)
Exclusion Criteria:
- History of allergy to study drugs, or previous history of allergy to sulpha drugs
- History or presence of major illnesses likely to influence pregnancy outcome
including diabetes mellitus, severe renal or heart disease, or active tuberculosis,
prior to randomization;
- Any significant illness that requires hospitalization;
- Intent to move out of the study catchment's area before delivery or deliver at
relative's home out of the catchment's area;
- Prior enrolment in the study or concurrent enrolment in another study
- Severe anaemia (Hb<7 g/dl)
- Previous history of unfavourable pregnancy outcome: pre-eclampsia, caesarean section,
stillbirth.
- Being HIV infected and already receiving CTX prophylaxis or ARV treatment
Locations and Contacts
Choma hospital, Choma, Zambia
Shampande Clinic, Shampande, Zambia
Additional Information
study results
Starting date: February 2009
Last updated: June 4, 2014
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