PACTR201308000543272Completed未知
Intermittent preventive treatment versus intermittent screening and treatment of malaria in pregnancy
niversity of Calabar0 sites460 target enrollmentStarted: April 29, 2013Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 460
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 15 Year(s) to 49 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •Pregnancy (16-24 weeks gestation) confirmed at first booking
- •Willing to have supervised delivery
- •Permanent residence within the study area
Exclusion Criteria
- •Haemoglobin < 6.0 g/dl or haematocrit of <18%
- •Presence of malaria requiring parenteral medication or parasite density ¿ 100,000/mm3 of blood.
- •Past obstetric and medical history that will adversely affect the evaluation of outcomes.
- •A prior dose of SP-IPTp
- •Sensitivity to SP, lumefantrine or an artemisinin
- •An illness requiring hospital admission.
- •Known G6PD deficiency to exclude women at risk of haemolytic anaemia.
- •Women who are known to be HIV infected before enrollment will not be recruited because, according to World Health Organization (WHO) and national recommendations, they should receive 3 (rather than 2) IPTp doses.
- •Failure to meet any of the inclusion criteria stated above.
Investigators
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