Actively Recruiting

Age: 18Years +
FEMALE
ID07336017

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - Up to 3 months before or after staff training

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

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

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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

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