CompletedPhase 4ACTRN12611000638932
Impact of pre-operative misoprostol on blood loss during and after elective cesarean delivery.
Sponsor
Mervat Sheikh Elarab Elsedeek Omran
Enrollment
400 participants
Start Date
Jan 1, 2008
Study Type
Interventional
Conditions
Summary
The primary purpose of this study was to evaluate the efficacy of rectal misoprostol in reducing blood loss during and after cesarean delivery.
Eligibility
Sex: Females
Plain Language Summary
Simplified for easier understanding
This study tests whether giving misoprostol before a planned cesarean delivery can reduce blood loss during and after the surgery. It focuses on women with full-term pregnancies who are scheduled for elective cesarean sections.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
preoperative adminstration of 400 microgram rectal misoprostol immediately before skin incision.
preoperative adminstration of 400 microgram rectal misoprostol immediately before skin incision.
Locations(1)
View Full Details on ANZCTR
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ACTRN12611000638932