drugset / Trial / NCT00124540
Misoprostol for Preventing Postpartum Hemorrhage
Completed
1200 enrolled
Gynuity Health Projects
Effective Care Research Unit · collabFamily Care International · collabUniversity of Witwatersrand, South Africa · collab
RandomizedParallel-groupTriple-blindPrevention
Summary
This hospital-based, multicenter, randomized, placebo-controlled trial will assess the effects of misoprostol as part of active management of the third stage of labor on postpartum blood loss, complications, and side effects. Twelve hundred eligible women will receive routine oxytocics (oxytocin 5-10 IU) plus either 400 mcg sublingual misoprostol or placebo during or immediately after delivery. The primary outcome will be measured blood loss of =\>500 mls within one hour after enrollment.
Timeline
- Start
- 2005-08
- Primary completion
- 2007-09
- Completion
- 2007-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Misoprostol | Other / unclassified | 400 ug | Other |
Indications
No indication recorded.