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Contribution of Ultrasonography in the Evaluation of Cervical Induction-delivery Time

Apport de l'échographie du Col Dans l'évaluation du Délai Induction Accouchement (DIA) Chez Des Patientes à Score de Bishop défavorable après déclenchement Par Dinoprostone Intravaginal

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02570620
Acronym
ECOLDIA
Enrollment
342
Registered
2015-10-07
Start date
2010-09-30
Completion date
2014-03-31
Last updated
2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Birth; Induced, Delivery Uterine

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.

Interventions

DEVICEUltrasonography of the cervix

Sponsors

University Hospital, Tours
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Time in hours between induction of prostaglandins and deliveryOn the day of inclusion after induction of prostaglandins. In relation to the time of delivery.Delivery whether a vaginal delivery or cesarean

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026