Double Simultaneous Uterotonic Agents Versus Single Agent Regimen to Prevent Early Postpartum Hemorrhage
Stony Brook University · NCT05245227
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 3
- Target enrollment
- 1358
- US sites recruiting
- 1
- Study start
- January 27, 2025
- Record last updated
- May 4, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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).
Being studied: Sublingual Misoprostol; IV Oxytocin
Conditions: Postpartum Hemorrhage
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
Stony Brook University
Stony Brook, NY 11794
Site contact: Erin Cassella · 631-444-7650 · erin.casella@stonybrookmedicine.edu
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