CClinicalTrials.gg
RecruitingNCT07336017IIA-LOSAUpdated Jan 13, 2026

Impact on Postpartum Anal Incontinence of an Educational Program for Delivery Room Staff

An observational study in Anal Incontinence, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-13.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 3 months later.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
1,000
Ages
18 Years and older
Sex
Female
01

Study summary

Obstetric anal sphincter injuries are a source of significant short-term (pain, bleeding, infection, suture dehiscence), medium-term (anorectovaginal fistulas, sexual dysfunction), and long-term (anal incontinence in 30-60% of cases) morbidity. However, they are underdiagnosed and sometimes poorly repaired due to technical difficulties, the use of inappropriate surgical techniques, or a lack of awareness of their significant long-term morbidity. These diagnostic and therapeutic errors, however, significantly worsen the functional prognosis of patients. This study aims to evaluate the clinical impact of an educational program designed for continuing education in the diagnosis and repair of obstetric anal sphincter injuries for staff working in the delivery room.

02

Conditions studied

  • Anal Incontinence

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Keywords

  • Anal Incontinence
  • Postpartum Anal Incontinence
  • Obstetric Anal Sphincter Injuries
03

In context

Encopresis

34 studies on the registry are indexed under Encopresis; 12 are open to participants now.

Browse Encopresis studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 966 studies on the registry; 342 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult women (≥18 years old) who gave birth vaginally at Strasbourg University Hospital in the 3 months prior to and 3 months following the training of delivery room staff at both maternity wards

Inclusion criteria

  • Adult women (≥18 years old)
  • who gave birth vaginally at Strasbourg University Hospital in the 3 months prior to and 3 months following the training of delivery room staff at both maternity wards
  • Singleton pregnancy
  • Live birth

Exclusion criteria

Exclusion Criteria:

  • Multiple pregnancy
  • Fetal death in utero
  • Medical termination of pregnancy
  • Delivery by cesarean section.
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
1,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. St. Mark's score

    The St Mark's score is a tool for measuring the severity of fecal incontinence: The score is based on several criteria: Solid leakage: 2 points (1-3 times per month) Liquid leakage: 3 points (once a week) Gas: 1 point (less than once a week) Protection: 1 point (occasionally) Daily life: 2 points (moderate discomfort) Ability to control: 1 point The points for each criterion are added together: * Minimum score = 0 → no incontinence. * Maximum score = 24 → very severe incontinence

    Time frame: Up to 18 months

07

Study locations

1 of 1 sites recruiting
  • Service de Gynécologique et d'Obstétrique - CHU de Strasbourg - France
    Strasbourg, 67091, France
    • Lise LECOINTRE, MD · Contact · lise.lecointre@chu-strasbourg.fr · 33 3 88 12 74 72
    • Lise LECOINTRE, MD · Principal investigator
    • Lucie VOGT-SCHILB, MD · Principal investigator
    • Eva FUSS, MD · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07336017
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Jan 13, 2026
Start date
Jun 17, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 17, 2026 (estimated)
Last update
Jan 13, 2026

Study contacts

Lise LECOINTRE, MD
Contact
lise.lecointre@chu-strasbourg.fr
33 3 88 12 74 7

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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