Contribution of Ultrasonography in the Evaluation of Cervical Induction-delivery Time (ECOLDIA)

Regional University Hospital Center (CHRU)

Status: Completed

Conditions: Delivery Uterine; Birth; Induced

Treatments: Device: Ultrasonography of the cervix

Study type: Interventional

Funder types: Other

Identifiers

NCT02570620

PHRI09-JP/ECOLDIA

Details and patient eligibility

About

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.

Enrollment: 342 patients

Sex: Female

Ages: 18 to 50 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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342 participants in 1 patient group

Observational cohort of patients

Experimental group

Description:

Patients will benefit from an ultrasonography of the cervix through endovaginal before induction of prostaglandins

Treatment:

Device: Ultrasonography of the cervix