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Effectiveness of Perineorrhaphy in Pelvic Organ Prolapse Surgery

NCT07006129 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40646

Last updated 2025-06-05

No results posted yet for this study

Summary

This is an observational registry-based study of long-term outcome after vaginal native tissue repair for pelvic organ prolapse designed to emulate a pragmatic open-label two-arm trial for which patients, in whom perineorrhaphy is not strictly indicated but clinically tenable, perioperatively are randomized to concomitant perineorrhaphy or not.

Conditions

  • Pelvic Organ Prolapse Vaginal Surgery
  • Pelvic Organ Prolapse (POP)

Interventions

PROCEDURE

Perineorrhaphy

Concomitant perineorrhaphy

PROCEDURE

No perineorrhaphy

No concomitant perineorrhaphy

Sponsors & Collaborators

  • Lund University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-01
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Sweden

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 NCT07006129 on ClinicalTrials.gov