Status:
UNKNOWN
Assessing a Predicted Time to Delivery in the Context of Cervical Ripening With Dinoprostone Vaginal Insert
Lead Sponsor:
University Hospital, Angers
Conditions:
Dinoprostone Vaginal Insert
Eligibility:
FEMALE
Brief Summary
Induction of labor is a common obstetric procedure that is routinely performed worldwide. However, when cervical conditions are not favorable (bishop \<6), induction of labor is preceded by cervical r...
Detailed Description
This is a before-after, retrospective and prospective monocentric study. Patients in the "before" group were part of another study which are currently in the process of publishing and were retrospecti...
Eligibility Criteria
Inclusion
- have cervical ripening with the dinoprostone vaginal insert
- 34 weeks gestational age (GA) and beyond
- singleton pregnancies
- cephalic presentations
Exclusion
- term \< 34 weeks GA
- previous history of cesarean section
- women who refuse to participate in the study or have their data used.
- twin pregnancy
- prostaglandin allergies
Key Trial Info
Start Date :
April 1 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 1 2019
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT03482531
Start Date
April 1 2018
End Date
November 1 2019
Last Update
May 30 2018
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Angers University hospital
Angers, Maine Et Loire, France, 49000