Clinical Trials Directory

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

TypeNameDescription
DRUGmisoprostol400 microgram of misoprostol is given preoperatively in patients undergoing elective cesarean section
DRUGplaceboowomen 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.

Could Pre-operative Rectal Misoprostol Reduce Intra-operative Blood Loss During Ceserean Section? (NCT02509351) · Clinical Trials Directory