Trials / Completed
CompletedNCT02509351
Could Pre-operative Rectal Misoprostol Reduce Intra-operative Blood Loss During Ceserean Section?
Randomized, Placebo-controlled Double Blind Study of Preoperative Misorostol for Reduction of Intraoperative Bleeding in Women Delivered by Ceserean Section
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 280 (actual)
- Sponsor
- Ain Shams University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
* Misoprostol reduces the uterine bleeding after cesarean delivery without harmful effects on either mother or baby. * The aim of the this study is to address if there is any benefits 'regarding the intra-operative blood loss' from preoperative rectal administration of 400 mic of Misoprostol in addition to the routinely administrated 10 units of oxytocin
Detailed description
Research question: In women undergoing elective ceserean section, is preoperative 400 mic Misoprostol reduce intra-operative blood loss? Research hypothesis: pre-operative Misoprostol doesn't reduce intraoperative blood loss in women undergoing ceserean section
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | misoprostol | 400 microgram of misoprostol is given preoperatively in patients undergoing elective cesarean section |
| DRUG | placeboo | women will recive 2 identical tablets as placeboo |
Timeline
- Start date
- 2015-10-01
- Primary completion
- 2016-11-01
- Completion
- 2016-11-01
- First posted
- 2015-07-28
- Last updated
- 2016-11-10
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT02509351. Inclusion in this directory is not an endorsement.