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New combo approach aims to ease pain after gallbladder surgery

NCT ID NCT07653490

Symptom relief Sponsor: Taksim Egitim ve Arastirma Hastanesi 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 1 time

Summary

This study tests whether a nerve block (erector spinae plane block) combined with low-flow anesthesia can improve recovery and reduce opioid use after laparoscopic gallbladder removal. 72 adults aged 18-65 will be randomly assigned to receive either the nerve block plus low-flow anesthesia or standard care. The main goal is to see if patients feel better 24 hours after surgery, with less pain and fewer side effects.

What this could mean

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

Active substance
bupivacaine
What this could lead to
If this works, it could offer a way to reduce pain and opioid use after gallbladder surgery, leading to a smoother recovery.
What could go wrong
This is a small, early-stage study with only 72 participants. The results may not apply to everyone, and the nerve block carries risks like infection or allergic reaction.

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 72 people

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

Started

Jun 2026

Expected to finish

Jun 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.

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: * Patients aged 18-65 years * ASA physical status I-II * Body mass index (BMI) \<35 kg/m² * Scheduled for elective laparoscopic cholecystectomy * Ability to provide written informed consent Exclusion Criteria: * Coagulopathy or bleeding disorders * Allergy to local anaesthetic agents * Infection at the block application site * Neurological or psychiatric disorders * Communication difficulties * Chronic opioid or analgesic use * Reoperation cases * Acute cholecystitis * Conversion to open surgery * Inadequate dermatomal block after ESPB * Severe intraoperative hemodynamic instability * Intraoperative blood loss ≥250 mL * Development of allergic reactions or major complications during follow-up

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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 cholecystectomy Postoperative pain

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

  • Taksim Training and Research Hospital

    RECRUITING

    Istanbul, 34000, Turkey (Türkiye)

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