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New trial pits two key surgeries against each other for Post-Hysterectomy prolapse

NCT ID NCT07174921

Disease control Sponsor: Kanuni Sultan Suleyman Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study compares two laparoscopic surgeries—lateral suspension and sacrocolpopexy—for women with vaginal cuff prolapse after hysterectomy. Fifty women will be randomly assigned to one surgery, and researchers will track recurrence, complications, recovery, and satisfaction. The goal is to identify which approach is safer and more effective.

What this could mean

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

Active substance
Laparoscopic surgery (lateral suspension or sacrocolpopexy) with synthetic mesh
What this could lead to
If this trial succeeds, it could show which surgical technique is better for fixing vaginal cuff prolapse, helping doctors and patients choose the safest, most effective option.
What could go wrong
This is a small, early-stage trial with only 50 participants, so results may not apply to everyone. Both surgeries carry risks like mesh exposure, infection, or injury.

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 50 people

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

Expected to start

Sep 2025

An estimate. Start dates often move.

Expected to finish

Oct 2026

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: Women aged ≥18 years. History of hysterectomy (any approach: abdominal, vaginal, or laparoscopic). Symptomatic vaginal cuff prolapse (POP-Q stage ≥ II). Able to provide written informed consent. Willing and able to comply with study procedures and follow-up visits. Exclusion Criteria: Prior sacrocolpopexy or lateral suspension surgery. Active pelvic infection or untreated malignancy. Severe cardiopulmonary or systemic disease that contraindicates laparoscopic surgery. Known allergy to mesh materials used in the procedures. Inability to complete patient-reported questionnaires due to cognitive or language barriers. Concurrent pelvic organ prolapse requiring additional surgical repair beyond vaginal cuff suspension.

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Conditions

The condition(s) this trial relates to.

pelvic organ prolapse Prolapse prolapse of female genital organ

As listed by the trial registrant

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

Vaginal cuff complications

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

  • Basaksehir Cam and Sakura City Hospital

    RECRUITING

    Istanbul, Istanbul, 34494, Turkey (Türkiye)

More trials for these conditions

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