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. 2016 Apr 14;2016(4):CD011491. doi: 10.1002/14651858.CD011491.pub2

NCT01713153.

Methods RCT.
Participants Women delivering in community health centres (case de sante) with a trained study provider (matrone) who are able to provide informed consent.
Interventions Misoprostol 600 mcg misoprostol orally versus UnijectTM 10 IU oxytocin delivered intramuscularly with UnijectTM.
Outcomes Mean change in haemoglobin.
Notes The recruitment status of this study is unknown because the information has not been verified recently in ClinicalTrials.gov.

IU: international unit
 mcg: microgram
 PHC: primary health centre
 RCT: randomised controlled trial