Status:
ACTIVE_NOT_RECRUITING
IC-CS Risk: Patient Outcomes
Lead Sponsor:
University of Pennsylvania
Collaborating Sponsors:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Conditions:
Cesarean Delivery
Eligibility:
FEMALE
Phase:
NA
Brief Summary
This study is looking at the impact of the implementation of a cesarean risk calculator on cesarean delivery and maternal morbidity rates.
Detailed Description
In this study a cesarean risk calculator will be instituted as a part of standard of care in a randomized rollout at 14 labor and delivery clinical sites across 4 institutions. The leadership at all o...
Eligibility Criteria
Inclusion
- All postpartum patients who were eligible for cesarean risk calculator utilization:
- delivery of a full-term (greater than or equal to 37 weeks) singleton gestation after presenting
- with intact membranes
- undergoing an induction of labor from cervical dilation less than or equal to 2cm
Exclusion
- Postpartum patient who had a prior pregnancy resulting in Cesarean delivery
Key Trial Info
Start Date :
September 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2027
Estimated Enrollment :
20000 Patients enrolled
Trial Details
Trial ID
NCT06488092
Start Date
September 1 2024
End Date
September 1 2027
Last Update
September 10 2025
Active Locations (14)
Enter a location and click search to find clinical trials sorted by distance.
1
University of Michigan
Ann Arbor, Michigan, United States, 48109
2
Henry Ford Macomb Hospital
Clinton Township, Michigan, United States, 48038
3
Henry Ford Hospital
Detroit, Michigan, United States, 48202
4
E.W. Sparrow Hospital
Lansing, Michigan, United States, 48912