Malaria Pregnancy and Childbirth
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Pregnancy (16-24 weeks gestation) confirmed at first booking Willing to have supervised delivery Permanent residence within the study area
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevalence of severe maternal anaemia (Hb < 8g/dl) of gestation | — |
Secondary
| Measure | Time frame |
|---|---|
| Prevalence of low birth weight (< 2500g) ;Prevalence of maternal anaemia (Hb < 11g/dl);Prevalence of placental malaria;Prevalence and density of microscopical and sub-microscopical gametocytamia;Prevalence and density of maternal parasitaemia;Congenital anomalies in live births;Prevalence of neonatal mortality;Prevalence of maternal mortality;Proportions of spontaneous abortions, intrauterine deaths, stillbirths, and pre-term deliveries | — |
Countries
Nigeria
Contacts
Lecturer