Evaluation of the Impact of Rotating Posterior and Transverse Presentations At 2 Hours of Full Dilation
NCT ID: NCT06886854
Last Updated: 2025-03-20
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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ACTIVE_NOT_RECRUITING
1000 participants
OBSERVATIONAL
2024-09-01
2025-12-01
Brief Summary
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Our study aims to demonstrate the benefits of manual rotation two hours after full dilation. This delay allows 90% of fetuses to rotate spontaneously, and it could help harmonize obstetrical practices.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Success of the rotation
Patients in labor with a fetus in posterior or transverse position at 2 hours of full dilation, verified by ultrasound. Manual rotation by an obstetrician after confirming effective analgesia, an empty bladder, and normal fetal heart rate. Success of the manual rotation
Mode of delivery
Retrieval of delivery data, typically recorded by midwives - retrieval of data per delivery and post-delivery - Consultation of medical data on labor duration, labor onset method, estimated fetal weight, etc.
Data collected for each delivery, identical in both groups.
Interventions
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Mode of delivery
Retrieval of delivery data, typically recorded by midwives - retrieval of data per delivery and post-delivery - Consultation of medical data on labor duration, labor onset method, estimated fetal weight, etc.
Data collected for each delivery, identical in both groups.
Eligibility Criteria
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Inclusion Criteria
* Low-pitched voice agreement
* Mobile fetal cephalic presentation
* Transverse or posterior presentation confirmed by ultrasound
* 2 hours of complete dilation
* Agreement for 3 hours by OB-GYN
* Normal fetal heart rate
* Epidural anesthesia in place
* Bladder catheterized
Exclusion Criteria
* Breech presentation
* Fetus \> 5000 g
* Patient refusal
* Inadequate analgesia
* Fetal hypoxia
15 Years
50 Years
MALE
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Hopital de la croix rousse
France, , France
Hopital Femme Mere Enfant
France, , France
Countries
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Other Identifiers
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24-5373
Identifier Type: -
Identifier Source: org_study_id
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