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The Effect of Misoprostol Given Preoperative Versus Postoperative on Blood Loss With Elective Cesarean Section: Randomized Controlled Trial
comparison of the effect of misoprostol before and after cesarean on the blood loss
70 women who received 600 mg misoprostol rectally preoperatively versus 70 women who received 600 mg misoprostol postoperatively at operating theatre
Age
20 - 35 years
Sex
FEMALE
Healthy Volunteers
No
Kasr El Ainiy Hospital
Cairo, Egypt
Start Date
March 1, 2018
Primary Completion Date
September 1, 2018
Completion Date
September 1, 2018
Last Updated
March 13, 2018
140
ESTIMATED participants
rectal misoprostol 600mg
DRUG
Lead Sponsor
sarah mohamed hassan
NCT05370820
NCT05977686
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06513351