Changes in Hemorrhage With Prophylactic Oxytocin for Dilation and Evacuation
University of Colorado, Denver · NCT06141447
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 18–55 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 2
- Target enrollment
- 150
- US sites recruiting
- 1
- Study start
- May 2, 2024
- Record last updated
- December 10, 2024
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to assess the effectiveness of prophylactic oxytocin on hemorrhage rates for second trimester dilation and evacuation (D\&E) in the clinic setting.
Being studied: Oxytocin + normal saline; Normal saline
Conditions: Hemorrhage
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- clinic-based D\&E at 18 weeks gestational age and above
- speaks English or Spanish
Exclusion Criteria
- refuses IV
- history of coagulopathy
- anticoagulant use in the preceding five days
- chorioamnionitis or sepsis
- suspected placenta accreta spectrum
- intrauterine fetal demise
- multiple gestation
- use of misoprostol for cervical preparation
Recruiting US locations
Comprehensive Women's Health Center
Denver, CO 80230
Site contact: Megan Masten, MD
Study contacts (from the official record)
- Megan Masten, MD · 303-724-8576 · megan.masten@cuanschutz.edu
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