Overview
Double Simultaneous Uterotonic Agents Versus Single Agent Regimen to Prevent Early Postpartum Hemorrhage
Status:
Recruiting
Recruiting
Trial end date:
2025-01-01
2025-01-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
To determine the effectiveness of using two medications simultaneously versus one medication, as is standard of care, in preventing early postpartum hemorrhage. There have been studies that looked at giving two medications and that there were reduced odds of postpartum hemorrhage. Specific Aim 1: Determine if double simultaneous uterotonic agent regimen (misoprostol and oxytocin) is superior to single agent (oxytocin only) in reducing postpartum hemorrhage. Specific Aim 2: Determine any potential side effects of a double simultaneous uterotonic agentregimen (misoprostol and oxytocin) versus a single agent (oxytocin only).Phase:
Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Stony Brook UniversityTreatments:
Misoprostol
Oxytocin
Criteria
Inclusion Criteria:- All women 18 years and older admitted to delivery at Stony Brook University hospital who
agree to participate in the study
Exclusion Criteria:
- Women under 18 years old
- Women with known coagulation disorders
- Women with planned cesarean hysterectomy
- Women with known placental accreta spectrum disorders
- Women with known allergy to prostaglandins