IC-CS Risk: Patient Outcomes

Running, not enrolling · Not applicable

Conditions studied: Cesarean Delivery

In brief

This study is looking at the impact of the implementation of a cesarean risk calculator on cesarean delivery and maternal morbidity rates.

Key facts

Study ID

NCT06488092

Run by

University of Pennsylvania

People needed

20000

Starts

2024-09-01

Expected to finish

2027-09-01

Last updated by the study team

2025-09-10

Who can join

Age: any. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• Postpartum patient who had a prior pregnancy resulting in Cesarean delivery

Where it is running

• University of Michigan — Ann Arbor, Michigan, United States
• Henry Ford Macomb Hospital — Clinton Township, Michigan, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• E.W. Sparrow Hospital — Lansing, Michigan, United States
• Princeton Medical Center — Plainsboro, New Jersey, United States
• Akron General — Akron, Ohio, United States
• Fairview Hospital — Cleveland, Ohio, United States
• Hillcrest Hospital — Mayfield Heights, Ohio, United States
• Lancaster General Health — Lancaster, Pennsylvania, United States
• Chester County Hosptial — West Chester, Pennsylvania, United States
• Logan Regional Hospital-Intermountain Healthcare — Logan, Utah, United States
• McKay-Dee Hospital — Ogden, Utah, United States
• Riverton Hospital-Intermountain Healthcare — Riverton, Utah, United States
• University of Utah Hospital — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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