Contribution of Ultrasonography in the Evaluation of Cervical Induction-delivery Time
Not Applicable
Completed
- Conditions
- Delivery UterineBirth; Induced
- Interventions
- Device: Ultrasonography of the cervix
- Registration Number
- NCT02570620
- Lead Sponsor
- University Hospital, Tours
- Brief Summary
Study of the contribution of ultrasound measurements of the uterine cervix related to the calculation of Bishop score. Evaluation of the period between cervical induction and delivery. Study of ultrasound data to improve the care of these patients requiring induction.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 342
Inclusion Criteria
- Age > 18 years
- Single pregnancy to term (> 37 weeks) in cephalic presentation
- Bishop score on the day of inclusion equal to 4.5 or 6
- Medical indication in accordance with professional recommendations of the April 2008 HAS.
Exclusion Criteria
- Cicatricial uterus
- Placenta previa
- Parity > 3 (more than 3 previous deliveries > 22 weeks)
- History of cone biopsy and strapping
- Known fetal malformation
- Known allergy to prostaglandins
- Woman under guardianship
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Observational cohort of patients Ultrasonography of the cervix Patients will benefit from an ultrasonography of the cervix through endovaginal before induction of prostaglandins
- Primary Outcome Measures
Name Time Method Time in hours between induction of prostaglandins and delivery On the day of inclusion after induction of prostaglandins. In relation to the time of delivery. Delivery whether a vaginal delivery or cesarean
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
University Hospital of Nantes
🇫🇷Nantes, France
Hospital of Orleans
🇫🇷Orleans, France
University Hospital of Tours
🇫🇷Tours, France