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A simple diet and muscle relaxant may sharpen views in scarless hysterectomy

NCT ID NCT07730970

Symptom relief Sponsor: Fatih Sultan Mehmet 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 28, 2026 · Last updated Jul 31, 2026 · Updated 3 times

Summary

This trial tests whether a three-day low-residue diet and deeper muscle relaxation, alone or together, can improve the surgical view during vNOTES hysterectomy (a scarless procedure through the vagina). The study involves 160 women having hysterectomy for non-cancer conditions. Researchers will measure the lowest gas pressure needed for a clear view, aiming to see if the combination works better than either approach alone.

What this could mean

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

Active substance
rocuronium (a muscle relaxant) and a low-residue diet
What this could lead to
If the combination works, surgeons may get a clearer view during vNOTES hysterectomy without needing higher gas pressure, potentially reducing complications.
What could go wrong
This is a small, early-stage trial with 160 participants. The benefits may be modest or not apply to all patients. Deeper muscle relaxation carries risks like prolonged recovery or side effects from the reversal drug.

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 160 people

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

Started

Jul 2026

Expected to finish

Sep 2027

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: * Adult women (aged 18 years or older) scheduled for hysterectomy for a benign (non-cancer) indication. * Judged suitable for the vNOTES approach by the operating surgeon. * Able to understand the study and provide written informed consent. Exclusion Criteria: * Suspected or known gynaecological malignancy. * Conditions expected to make the approach or the field assessment non-standard (e.g., anticipated dense pelvic adhesions or severe endometriosis, a contraindication to vNOTES, or an obliterated cul-de-sac). * Any medical reason why deep neuromuscular blockade or sugammadex would be unsafe (defined with the anaesthesia team). * Any medical reason why a low-residue diet would be unsuitable. * Inability to give informed consent.

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Conditions

The condition(s) this trial relates to.

adenomyosis leiomyoma Metrorrhagia pelvic organ prolapse Pneumoperitoneum prolapse of female genital organ uterine corpus leiomyoma Uterine Prolapse

As listed by the trial registrant

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

Abnormal uterine bleeding (AUB) Adenomyosis of uterus Benign gynecological disease Leiomyoma, uterine Uterine prolapse

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

  • Acibadem Kartal Hospital

    RECRUITING

    Istanbul, KARTAL, Turkey (Türkiye)

  • Kartal Dr. Lütfi Kırdar Şehir Hastanesi

    ACTIVE_NOT_RECRUITING

    Istanbul, KARTAL, 34865, Turkey (Türkiye)

  • Kütahya Şehir Hastanesi

    ACTIVE_NOT_RECRUITING

    Kütahya, Kütahya, 43100, Turkey (Türkiye)

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