Discourse on the Mother's Decision Regarding the Mode of Delivery in Cases of Breech Presentation
NCT ID: NCT07314970
Last Updated: 2026-01-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2025-01-28
2026-02-28
Brief Summary
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Despite its frequency, breech presentation at term remains a subject of considerable controversy within the medical community regarding the management of labor. In the 2000s, a randomized trial called the TERM BREECH TRIAL found a neonatal benefit of planned cesarean section compared to vaginal delivery of a breech fetus (prevention of perinatal death in 1% of cases). This resulted in a significant increase in the rate of planned cesarean sections for breech presentation worldwide. However, numerous more recent studies (notably PREMODA in France) have highlighted the many biases of the Term Breech Trial, and various literature reviews (including the 2015 Cochrane review) have demonstrated lower perinatal morbidity than that found by Hannah's team. In 2020, the CNGOF (National College of Gynecologists and Obstetricians of France) published new recommendations on the management of breech presentations at the end of pregnancy, proposing vaginal delivery as a possible alternative to a planned cesarean section, provided that the patient receives clear and honest information (benefits and risks of each delivery method). The choice of delivery method must be made in consultation with the patient after a dedicated consultation. Since these recommendations were published, management practices still vary between hospitals despite fairly precise guidelines.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Doctor with a primary focus on Obstetrics
* Practicing in a University Hospital in the Grand Est region (Besançon, Reims, Strasbourg, Nancy)
* Agreeing to complete the self-administered questionnaire anonymously.
To complete a questionnaire
Doctor and Adult woman agreeing to complete the self-administered questionnaire anonymously.
Adult woman (≥ 18 years old)
* Gave birth in 2024 at a university hospital in the Grand Est region (Besançon, Reims, Strasbourg, Nancy)
* Breech delivery \> 37 weeks gestation
* Agree to complete the self-administered questionnaire anonymously.
To complete a questionnaire
Doctor and Adult woman agreeing to complete the self-administered questionnaire anonymously.
Interventions
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To complete a questionnaire
Doctor and Adult woman agreeing to complete the self-administered questionnaire anonymously.
Eligibility Criteria
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Inclusion Criteria
* Doctor with a medical degree (Junior Doctor, Clinical Assistant, Hospital Practitioner, University Professor of Obstetrics), with a primary focus on Obstetrics
* Practicing in a University Hospital in the Grand Est region (Besançon, Reims, Strasbourg, Nancy)
* Agreeing to complete the self-administered questionnaire anonymously.
Regarding patients:
* Patient of legal age (≥ 18 years)
* Having given birth in 2024 in a university hospital in the Grand-Est region (Besançon, Reims, Strasbourg, Nancy)
* Delivery of a breech fetus \> 37 weeks of gestation
* Agreeing to answer the self-administered questionnaire anonymously.
Exclusion Criteria
Other primary activity than obstetrics
Regarding patients:
* Minor patient at the time of delivery
* Patient who had a cesarean section due to a uterine scar and maternal desire.
* Patients with a history of uterine scarring or the presence of obstruction previa were also excluded due to the impossibility of authorizing vaginal delivery, regardless of fetal presentation.
18 Years
ALL
No
Sponsors
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University Hospital, Strasbourg, France
OTHER
Responsible Party
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Locations
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Service de Gynécologique et d'Obstétrique - CHU de Strasbourg - France
Strasbourg, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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9537
Identifier Type: -
Identifier Source: org_study_id
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