Daily Co-trimoxazole Prophylaxis to Prevent Malaria in Pregnancy

Sponsor

Institute of Tropical Medicine, Belgium (Other)

Overall Status

Terminated

CT.gov ID

NCT00711906

Collaborator

Tropical Diseases Research Centre, Zambia (Other)

352

Enrollment

Locations

Arms

Duration (Months)

176

Patients Per Site

9.3

Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Malaria in Pregnancy	Drug: Cotrimoxazole Drug: Sulfadoxine-pyrimethamine	Phase 3

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.

Study Design

Study Type:

Interventional

Actual Enrollment :

352 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Prevention

Official Title:

The Role of Daily Co-trimoxazole Prophylaxis For Prevention of Malaria And Its Effects in Pregnancy

Study Start Date :

Feb 1, 2009

Actual Primary Completion Date :

Feb 1, 2010

Actual Study Completion Date :

Sep 1, 2010

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 1 HIV-negative women taking CTX as chemoprophylaxis	Drug: Cotrimoxazole Cotrimoxazole Other Names: CTX Bactrim
Active Comparator: 2 HIV-negative women taking SP as IPT	Drug: Sulfadoxine-pyrimethamine Sulfadoxine-pyrimethamine Other Names: SP Fansidar
Experimental: 3 HIV-positive women (CD4> 200) taking CTX as chemoprophylaxis	Drug: Cotrimoxazole Cotrimoxazole Other Names: CTX Bactrim
Active Comparator: 4 HIV-positive women (CD4 > 200) taking SP as IPT	Drug: Sulfadoxine-pyrimethamine Sulfadoxine-pyrimethamine Other Names: SP Fansidar

Outcome Measures

Primary Outcome Measures

To test the hypothesis that co-trimoxazole prophylaxis is not inferior to SP intermittent preventive treatment in preventing placental malaria. [Pregnancy]

Secondary Outcome Measures

To evaluate efficacy of CTX prophylaxis in preventing malaria peripheral parasitaemia. [Pregnancy]
To evaluate efficacy of CTX prophylaxis in preventing perinatal mortality and in improving birth weight [At birth]
To establish the safety of CTX prophylaxis on the offspring by measuring the gestational age at delivery and birth weight. [At birth]
To compare the efficacy profile of CTX prophylaxis to that of SP intermittent preventive treatment. [Pregnancy]
To compare the safety profile of CTX prophylaxis to that of SP intermittent preventive treatment. [Pregnancy]
Spontaneous abortion [</=28 weeks gestation]
Pre-term delivery [<37 completed weeks]
Neonatal mortality [Within 28 days after birth]
Maternal mortality [Up to 6 weeks following delivery]
Major and minor birth defects [At birth and up to 6 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A and Older

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Choma hospital	Choma		Zambia
2	Shampande Clinic	Shampande		Zambia

Sponsors and Collaborators

Institute of Tropical Medicine, Belgium
Tropical Diseases Research Centre, Zambia

Investigators

Principal Investigator: Christine Manyando, MD, Tropical Diseases Research Centre
Study Director: Jean-Pierre Van geertruyden, MD PhD, Institute of Tropical Medicine