Trials / Unknown
UnknownNCT03463070
Misoprostol Before and After Cesarean Section
The Effect of Misoprostol Given Preoperative Versus Postoperative on Blood Loss With Elective Cesarean Section: Randomized Controlled Trial
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 140 (estimated)
- Sponsor
- sarah mohamed hassan · Academic / Other
- Sex
- Female
- Age
- 20 Years – 35 Years
- Healthy volunteers
- Not accepted
Summary
comparison of the effect of misoprostol before and after cesarean on the blood loss
Detailed description
70 women who received 600 mg misoprostol rectally preoperatively versus 70 women who received 600 mg misoprostol postoperatively at operating theatre
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | rectal misoprostol 600mg | 70 women who received 600 mg misoprostol postoperatively at operating theatre |
Timeline
- Start date
- 2018-03-01
- Primary completion
- 2018-09-01
- Completion
- 2018-09-01
- First posted
- 2018-03-13
- Last updated
- 2018-03-13
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT03463070. Inclusion in this directory is not an endorsement.