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Postoperative Vaginal Compression After Prolapse Surgery - an RCT

NCT07612202 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2026-05-28

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if omitting postoperative vaginal compression (packing) can facilitate a more efficient recovery after elective surgery for uterovaginal prolapse. The main questions it aims to answer are: Will the omission of vaginal compression result in a non-inferior (unchanged) rate of prolapse recurrence within the first three months after surgery? Does the omission of vaginal compression lead to a shorter hospital stay and a faster return of normal bladder function? Researchers will compare a group that receives no postoperative vaginal compression to a control group that receives standard vaginal gauze packing for two hours to see if skipping the packing leads to shorter hospital stays and faster bladder emptying without increasing the risk of the prolapse returning.

Conditions

  • Postoperative Care
  • Prolapse Genital
  • Urogynecologic Surgery

Interventions

OTHER

No postoperative vaginal compression

No vaginal compression through vaginal gauze packing after urogynecolocigal surgery

OTHER

Postoperative vaginal compression

Postoperative vaginal compression through vaginal gauze packing after urogynecolocigal surger

Sponsors & Collaborators

  • Nordsjaellands Hospital

    collaborator OTHER

  • Christiane Marie Bourgin Folke Gam

    lead OTHER

Principal Investigators

  • Christiane M. B. F. Gam, MD, PhD · Departement og Gynecology-Obstetrics, Copenhagen University Hospital - North Zealand

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-03
Primary Completion
2028-06-30
Completion
2028-12-31

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 NCT07612202 on ClinicalTrials.gov