drugset / Trial / NCT03144401
Preoperative vs. Postoperative Misoprostol in Elective Cesarean Section
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This prospective double-blind placebo-controlled randomized clinical trial will be conducted at Ain-Shams University Maternity Hospital from April 2017 till October 2017. 120 women candidate foe elective cesarean section will receive preoperative sublingual 400 microgram of misoprostol, and another 120 women will receive postoperative sublingual 400 microgram of misoprostol.
Timeline
- Start
- 2017-04-10
- Primary completion
- 2018-01-12
- Completion
- 2018-02-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Misoprostol | Other / unclassified | 400 ug | Other |
Indications
No indication recorded.