Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

No packing, faster healing? new trial questions routine after prolapse surgery

NCT ID NCT07612202

Symptom relief Sponsor: Christiane Marie Bourgin Folke Gam Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This trial tests if leaving out vaginal gauze packing after prolapse surgery helps women recover faster. 360 women having surgery for pelvic organ prolapse will be randomly assigned to either receive standard packing for two hours or no packing at all. The goal is to see if skipping packing leads to shorter hospital stays and quicker return of normal bladder function, without raising the risk of the prolapse coming back within three months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
vaginal gauze packing
What this could lead to
If successful, this could show that skipping vaginal packing after prolapse surgery shortens hospital stays and speeds up bladder recovery without increasing the risk of prolapse returning.
What could go wrong
This is a small, early-stage trial with only 360 participants, so results may not apply to all patients. The main risk is that omitting packing might lead to more prolapse recurrences.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 360 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: * Planned anterior colporrhaphy, posterior colporrhaphy, or cervical amputation at the day surgery department, Nordsjællands Hospital, Capital Region, Denmark * Age 18 years and older . Cognitively capable patient * Received information material as described in the protocol Exclusion criteria: * Failure to pause blood-thinning medication on the day of surgery, if this was planned * Failure to discontinue regular intake of fish oil or ginger extract four weeks prior to the procedure * Immunosuppressed patients * Planned perineorrhaphy * Surgery involving more than two compartments * Non-Danish speaking patients

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Postoperative care are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

pelvic organ prolapse prolapse of female genital organ

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Postoperative care Prolapse genital Urogynecologic surgery

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Department of Gynecology-Obstetrics, Copenhagen University Hospital - North Zealand

    Hillerød, Copenhagen, 3400, Denmark

More trials for these conditions

Other studies related to the condition(s) this trial covers.