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Gestational malaria in Kisangani: Efficacy of Mefloquine versus Sulfadoxine-Pyrimethamine in Intermittent Preventive Treatment

Not Applicable
Conditions
Pregnancy and Childbirth
Malaria
Registration Number
PACTR201905899965726
Lead Sponsor
niversity of Kisangani
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
300
Inclusion Criteria

Pregnant women who will :
- begin antenatal visits in medical facilities selected from gestational age between 16 and 18 weeks of amenorrhea,
- have not yet received SP prophylaxis during ongoing pregnancy
- sign their consent form.

Exclusion Criteria

Pregnant women with :
- positive HIV serology,
- story of morbid neurological and psychiatric,
- story of SP allergy
- of antimalarial drug(s) use within 15 days prior to selection will be excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
- Mefloquine will be well tolerated by Kisangani pregnant women;<br>- Mefloquine will be more effective than SP in pregnant women in Kisangani.<br>
Secondary Outcome Measures
NameTimeMethod
- Mefloquine Side-effects will be less frequent and minors, easy to control;<br>- The prevalence of maternal anemia at delivery will be lower among pregnant women who have taken the Mefloquine compared to those who will use Sulfadoxine-Pyrimethamine;<br>- Placental malaria parasitemia will be lower among pregnant women who have taken the Mefloquine compared to those who will use Sulfadoxine-Pyrimethamine;<br>- The prevalence of low birth will be lower among pregnant women who have taken the Mefloquine compared to those who will use Sulfadoxine-Pyrimethamine.
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