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New vaginal surgery may be easier on lungs and heart during operation

NCT ID NCT07667907

Knowledge-focused Sponsor: Bursa Yuksek Ihtisas 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will compare two types of minimally invasive gynecological surgeries: vNOTES (done through the vagina) and standard laparoscopy (done through small belly cuts). Researchers want to see which method causes less stress on the lungs and heart during the procedure. Thirty women scheduled for elective gynecological surgery will be observed, with half receiving each technique. The goal is to find a safer surgical approach.

What this could mean

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

What this could lead to
If vNOTES proves better for breathing and heart stability, it could become a preferred surgical method for gynecological procedures.
What could go wrong
This is a small, early observational study with only 30 participants, so results may not apply to everyone. It does not test long-term outcomes.

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.

Participants

About 30 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Who is studied

Adult female patients aged 18-75 years scheduled for elective gynecological surgery under general anesthesia.

Ages

18 to 75 years

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: * Female patients aged 18 to 75 years * Patients scheduled for elective gynecological surgery * Patients undergoing mechanical ventilation under general anesthesia * ASA physical status I-III * Patients providing written informed consent Exclusion Criteria: * Severe or uncontrolled chronic obstructive pulmonary disease, asthma, or other chronic pulmonary diseases * Cardiac arrhythmia * ASA physical status IV or above * Patients developing intraoperative hemodynamic instability * Patients receiving spinal or epidural anesthesia * Cases requiring conversion to laparoscopy or laparotomy * Patients refusing to participate

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Conditions

The condition(s) this trial relates to.

Pneumoperitoneum

As listed by the trial registrant

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

Hemodynamics Respiratory mechanics

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

  • Bursa Yuksek Ihtisas Training and Research Hospital

    Bursa, Yıldırım, 16350, Turkey (Türkiye)

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