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Which anesthesia helps you recover faster after gynecologic surgery?

NCT ID NCT07506798

Knowledge-focused Sponsor: Sakarya University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study looks at whether combining intravenous and inhaled anesthesia helps women recover better after gynecologic surgery compared to inhaled anesthesia alone. One hundred women aged 18-65 will be randomly assigned to one of the two methods. Their recovery will be measured using a questionnaire called QoR-15, which covers pain, comfort, emotions, and daily activities.

What this could mean

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

Active substance
Combined intravenous-inhalational anesthesia vs. inhalational anesthesia alone
What this could lead to
If one method proves better, it could guide anesthesiologists to choose the best approach for faster, smoother recovery after gynecologic surgery.
What could go wrong
This is a small, single-center study (100 patients) comparing routine methods, so results may not apply broadly. It measures recovery scores, not 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.

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 100 people

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

Started

Oct 2025

Expected to finish

Apr 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 to 65 years

Sex

Anyone

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: 1. Patients aged 18-65 years 2. Scheduled for elective gynecologic surgery at Sakarya University Faculty of Medicine Training and Research Hospital 3. Classified as ASA I-III 4. Able to understand and complete the QoR-15 questionnaire 5. Provided written informed consent Exclusion Criteria: 1. Severe comorbidities (beyond ASA III) 2. Patients with advanced neurological disease or cognitive impairment 3. Known allergy to anesthetic drugs used in the study 4. Classified as ASA IV-V 5. Refusal to participate in the study 6. Emergency or urgent surgery

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As listed by the trial registrant

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

Anesthesia Gynecologic surgery Postoperative recovery

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

  • Sakarya University Training and Research Hospital

    RECRUITING

    Sakarya, 54290, Turkey (Türkiye)

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