Process for decision-making, obstetrical risk management and mode of delivery after a prior cesarean delivery in Québec

Not Applicable

Completed

• Conditions: Choice of mode of delivery among women with one prior cesarean delivery; Pregnancy and Childbirth

• Registration Number: ISRCTN15346559
• Lead Sponsor: CHU de Québec Research Center

Brief Summary

2017 Protocol article in https://pubmed.ncbi.nlm.nih.gov/28931404/ protocol (added 15/01/2021) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/38096892/ (added 15/12/2023)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-08-20
• Study Completion: 2020-09-30
• Last Update Posted: 8 January 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 24500

Inclusion Criteria

Hospital level:
1. Public hospitals with functional surgical rooms and high performance sonographic devices.
2. More than 300 deliveries per year
3. Written agreement to participate in the study from the directors of maternity services and professional services

Woman level (data collection):
1. All women with one prior cesarean delivery who delivered at participating centers and whose newborns had a gestational age of at least 22 weeks and weighed at least 500 g at delivery.

Exclusion Criteria

Hospital level:
1. Public hospitals with, at the time of recruitment, recent or ongoing quality-improvement programs specifically designed to target women with one prior cesarean delivery
Woman level (data collection):
2. Women that give birth or abort before 22 weeks of gestation

Study & Design

• Study Type: Interventional
• Study Design: Not specified