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Conservative Treatment or Resuturing Among Women With Perineal Wound Dehiscence After Vaginal Labour

NCT06026423 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2023-09-18

No results posted yet for this study

Summary

The goal of this observational study is to make us more aware of the short and long-term outcomes for women having an uncomplicated healing process after a rupture or birth cut in the perineum after giving birth in relation to a healing process with a dehisced wound treated with conservative management or secondary suturing.

Participants will be asked to do

* A gynecological examination at one month after birth and 9-12 months after birth.
* Have a picture taken of the healing process
* Answer a questionnaire at one month, three months, and 9-12 months after birth

Conditions

  • Dehiscence Wound
  • Secondary Perineal Tear
  • Episiotomy; Dehiscence

Interventions

OTHER

Clinical examination and pictures

A clinical examination is needed to assess the healing process for the three groups. After assessing the healing process, we will take pictures of the tear for documentation.

OTHER

Questionnaire

The participant will answer questions, serving as a baseline questionnaire, when arriving at the clinical examination one month post-partum. At three and 9-12 months post-postpartum, they will receive another questionnaire. The questionnaire will consist of validated questions regarding body image, pain, Urogynecological problems as symptoms of prolapse, urinary and anal incontinence, and questions about sexual problems.

Sponsors & Collaborators

  • Herlev Hospital

    lead OTHER

Principal Investigators

  • Hanna M. Jangö, MD, PhD · Copenhagen University Hospital - Herlev and Gentofte

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-15
Primary Completion
2024-09-01
Completion
2026-09-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06026423 on ClinicalTrials.gov