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New combo block may ease post-surgery pain better than standard approach

NCT ID NCT07264855

Symptom relief Sponsor: Bakirkoy Dr. Sadi Konuk Research and Training 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether combining two ultrasound-guided pain blocks (M-TAPA and EXOP) works better than M-TAPA alone for controlling pain after laparoscopic gynecologic surgery. About 86 women will have their pain scores, need for extra pain medicine, and recovery quality measured over 24 hours. The goal is to find a simple, drug-free way to improve comfort and recovery.

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 86 people

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

Started

Nov 2025

Expected to finish

Oct 2026

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 undergoing laparoscopic gynecologic surgery.

Ages

18 to 90 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: * Patients scheduled for laparoscopic gynecologic surgery * Age 18-90 years * ASA physical status I-III Exclusion Criteria: * Contraindications to block procedures (coagulopathy, anticoagulant therapy, local infection at needle insertion site, etc.) * Severe cardiac, renal, hepatic, hematologic, neurologic, or psychiatric disease * Allergy to amide-type local anesthetics * Chronic pain, narcotic or alcohol dependence * BMI ≥ 35 kg/m² * Pregnancy * Refusal to participate * Conversion from laparoscopy to laparotomy

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Laparoscopic gynecologic surgery Postoperative pain

Contacts and locations

Locations

  • SBÜ Bakırköy Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi

    Istanbul, Bakirkoy, 34147, Turkey (Türkiye)

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