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Effectiveness of two antifolate prophylactic strategies against malaria in HIV-positive pregnant women in Bangui, Central African Republic: study protocol for a randomized controlled trial (MACOMBA)
- Source :
- Trials, Trials, BioMed Central, 2013, 14 (1), pp.255. ⟨10.1186/1745-6215-14-255⟩, Trials, 2013, 14 (1), pp.255. ⟨10.1186/1745-6215-14-255⟩
- Publication Year :
- 2013
- Publisher :
- HAL CCSD, 2013.
-
Abstract
- International audience; BACKGROUND: Co-infection with malaria parasite and HIV is an emerging public health problem in tropical areas, particularly in pregnant women, and management of the concurrent effects of these two infections is challenging. Co-trimoxazole is a sulfamide preparation used to prevent opportunistic infections in HIV-infected patients, and many studies have reported that it has significant activity against malaria. As the efficacy of intermittent preventive treatment (IPT) with sulfadoxine-pyrimethamine (SP) against malaria is decreasing, co-trimoxazole might be an alternative for preventing malaria among HIV-infected populations. The aim of this study is to compare the effectiveness of SP-IPT, which is recommended for the prevention of malaria during pregnancy in the Central African Republic, with that of a daily dose of co-trimoxazole against P. falciparum infections among HIV-infected pregnant women in Bangui, the capital of the Central African Republic. METHODS/DESIGN: The MACOMBA study (MAternity and COntrol of Malaria-HIV co-infection in BAngui) is a multicentre open-label randomized clinical trial conducted at four maternity hospitals in Bangui. All HIV-infected pregnant women presenting for an antenatal clinic visit between the weeks 16 and 28 of amenorrhoea, with a CD4 count of more than 350 cells/mm3, will be eligible. All the women will provide written consent before being enrolled in the study and will then be randomly allocated to either SP-IPT (25 mg of sulfadoxine and 1.25 mg of pyrimethamine) or daily co-trimoxazole doses (960 mg per dose). The primary end-point is the placental malaria parasitaemia rate at delivery. Other main outcome measures include the number of malaria episodes during pregnancy, safety, and treatment compliance. Furthermore, the frequency of molecular resistance markers dhfr and dhps will be measured. DISCUSSION: In this trial, we seek to confirm whether co-trimoxazole is operationally suitable to replace SP-IPT in order to prevent malaria among pregnant women infected with HIV in the Central African Republic. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01746199.
- Subjects :
- Pediatrics
Time Factors
medicine.medical_treatment
Medicine (miscellaneous)
DHPS
HIV Infections
law.invention
chemistry.chemical_compound
Study Protocol
0302 clinical medicine
Randomized controlled trial
Clinical Protocols
law
Pregnancy
Pharmacology (medical)
030212 general & internal medicine
Malaria, Falciparum
Coinfection
Prenatal Care
3. Good health
Central African Republic
Drug Combinations
Pyrimethamine
Treatment Outcome
Research Design
Antifolate
Female
medicine.drug
medicine.medical_specialty
Sulfadoxine
Malaria prevention
030231 tropical medicine
Hospitals, Maternity
Drug Administration Schedule
03 medical and health sciences
Antimalarials
Trimethoprim, Sulfamethoxazole Drug Combination
parasitic diseases
medicine
Humans
business.industry
Public health
HIV
medicine.disease
chemistry
Pregnancy Complications, Parasitic
Immunology
Folic Acid Antagonists
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
business
Malaria
Subjects
Details
- Language :
- English
- ISSN :
- 17456215
- Database :
- OpenAIRE
- Journal :
- Trials, Trials, BioMed Central, 2013, 14 (1), pp.255. ⟨10.1186/1745-6215-14-255⟩, Trials, 2013, 14 (1), pp.255. ⟨10.1186/1745-6215-14-255⟩
- Accession number :
- edsair.doi.dedup.....e5036c9ff5fb22447c75c4d16be952b1