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Resident's journey to master scarless hysterectomy under the microscope

NCT ID NCT07465822

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 watches a single gynecology resident as they learn to perform a hysterectomy through the vagina using a special camera, leaving no belly scars. The goal is to see how quickly the resident improves, measuring surgery time and any complications. Nineteen women with benign uterine conditions will take part. The results could help design better training for this advanced technique.

What this could mean

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

Active substance
Vaginal Natural Orifice Transluminal Endoscopic Surgery (V-NOTES) hysterectomy
What this could lead to
If successful, this could help train surgeons more efficiently in a scarless hysterectomy technique, potentially reducing recovery time for patients.
What could go wrong
This is a small, observational study with only 19 patients, so results may not apply broadly. It focuses on a single resident's learning curve, not on comparing outcomes to standard surgery.

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 19 people

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

Started

Apr 2025

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.

Who is studied

Patients deemed suitable for V-NOTES hysterectomy based on preoperative evaluation

Ages

18 to 70 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: * Voluntary participation in the study and provision of written informed consent * Female patients aged between 18 and 70 years * Patients admitted to the Department of Obstetrics and Gynecology at Çukurova -University and scheduled for elective hysterectomy * Patients deemed suitable for V-NOTES hysterectomy based on preoperative evaluation Exclusion Criteria: * Refusal to provide informed consent * Anatomical or technical limitations preventing placement in the lithotomy -position * Pregnancy * Presence of acute abdomen or indication for emergency surgery * Presence or history of deep infiltrating endometriosis * Suspected pelvic adhesions * Detection of a nodule in the pouch of Douglas * Fixed uterus on pelvic examination * Sexually inactive patients * History of tubo-ovarian abscess

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Cukurova University

    Adana, 01000, Turkey (Türkiye)

More trials for these conditions

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