Actively Recruiting
Impact on Postpartum Anal Incontinence of an Educational Program for Delivery Room Staff on the Diagnosis and Repair of Obstetric Anal Sphincter Injuries
Led by University Hospital, Strasbourg, France · Updated on 2026-01-13
1000
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Obstetric anal sphincter injuries can cause significant short-term pain, bleeding, infection, and medium-term issues like sexual dysfunction, as well as long-term anal incontinence in up to 30-60% of cases. These injuries are often underdiagnosed or repaired incorrectly due to technical challenges and lack of awareness, which worsens patients' outcomes. This observational study aims to assess the clinical impact of an educational program for delivery room staff focused on improving the diagnosis and repair of these injuries. The study observes adult women who gave birth vaginally at Strasbourg University Hospital within a six-month window around the training of delivery room staff. Participants include those with singleton pregnancies and live births. The educational program is designed to enhance staff skills in managing obstetric anal sphincter injuries, though no specific interventions or treatments are administered to participants. Participants will be monitored for up to 18 months after delivery to assess outcomes using the St. Mark's score, which measures anal incontinence. The study involves follow-up evaluations to understand the long-term effects of improved staff training on postpartum anal incontinence. The total participation duration varies depending on the time since delivery and follow-up assessments.
CONDITIONS
Brief Title
Impact on Postpartum Anal Incontinence of an Educational Program for Delivery Room Staff
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult women (≥18 years old)
- Gave birth vaginally at Strasbourg University Hospital within 3 months before or after staff training
- Singleton pregnancy
- Live birth
You will not qualify if you...
- Multiple pregnancy
- Fetal death in utero
- Medical termination of pregnancy
- Delivery by cesarean section
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 3 months before or after staff training
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 18 months
Participants are monitored for postpartum anal incontinence up to 18 months after delivery.
Periodic assessments over 18 months
Trial Site Locations
Total: 1 location
1
Service de Gynécologique et d'Obstétrique - CHU de Strasbourg - France
Strasbourg, France, 67091
Actively Recruiting
Research Team
L
Lise LECOINTRE, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here