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Which pain block works best for hernia surgery? new trial aims to find out

NCT ID NCT07163026

Symptom relief Sponsor: Ankara Ataturk Sanatorium 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This trial compares two types of nerve blocks—erector spinae plane block and external oblique-intercostal plane block—for pain relief after open ventral hernia repair. Fifty adults scheduled for surgery will receive one of the two blocks, and researchers will measure how much extra painkiller they need in the first 24 hours. The goal is to find which block provides better pain control and reduces nausea and vomiting.

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 one block works better, it could mean less pain and fewer side effects after hernia surgery.
What could go wrong
This is a small, early-stage trial with only 50 people. Results may not apply to everyone, and individual responses to nerve blocks can vary.

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 50 people

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

Expected to start

Sep 2025

An estimate. Start dates often move.

Expected to finish

Dec 2025

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 scheduled for open ventral hernia repair under general anesthesia * Patients with ASA scores (American Society of Anesthesiologists) 1 and 2 * Patients with a body mass index between 18.5 and 34.9 Exclusion Criteria: * Patients scheduled for open ventral hernia repair under spinal or epidural anesthesia * Patients who have previously undergone spine surgery. * Patients with known local anesthetic allergy * Pregnant women * Mentally uncooperative patients * Patients with a history of chronic analgesic use

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Conditions

The condition(s) this trial relates to.

Hernia, Ventral Pain, Postoperative Postoperative Nausea and Vomiting

As listed by the trial registrant

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

Postoperative nausea Postoperative pain Postoperative vomiting Ventral hernia

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

  • Ankara Ataturk Sanatorium Research and Training Hospital

    Ankara, 06290, Turkey (Türkiye)

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