Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Can a targeted nerve block silence Post-Surgery pain?

NCT ID NCT06778629

Symptom relief Sponsor: Istanbul Medipol University 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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 04, 2026 · Last updated Aug 12, 2026 · Updated 3 times

Summary

This trial tests whether a specific nerve block, called a transversalis fascia plane block, can reduce pain after laparoscopic inguinal hernia repair. Sixty adults undergoing this surgery will receive the block, and researchers will measure their pain scores and painkiller use for 24 hours after the operation. The goal is to see if this block offers better pain control and a smoother recovery.

What this could mean

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

Active substance
Transversalis fascia plane block, a nerve block procedure using local anesthetic injected under ultrasound guidance
What this could lead to
If effective, this nerve block could become a standard way to reduce pain and the need for painkillers after laparoscopic hernia repair, improving recovery.
What could go wrong
This is a small, early-stage trial, and the block may not provide significant pain relief for everyone. There are also risks like infection, bleeding, or allergic reactions to the anesthetic.

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

60 people

The number who actually took part.

Started

Feb 2025

Finished

Jul 2026

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: * American Society of Anesthesiologists (ASA) classification I- II Patients * Unilateral Inguinal Hernia Repair Surgery * Elective Operations Exclusion Criteria: * Patients with a history of chronic pain * Evidence of infection in the intervention area * Allergy to local anesthetics * Coagulopathy * Body-mass index (BMI) ≥ 30 * Body weight ≤ 50 kg * Patients who do not agree to participate in the study

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Acute post operative pain are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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.

Acute post operative pain Laparoscopic inguinal hernia repair

Contacts and locations

Locations

  • Istanbul Medipol University Mega Hospital Complex

    Istanbul, Bagcilar, 34212, Turkey (Türkiye)

More trials for these conditions

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