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