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

Nerve block after hernia surgery may speed recovery

NCT ID NCT07509957

Symptom relief Sponsor: Sanliurfa Education 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 3 times

Summary

This study looks at whether a nerve block called an erector spinae plane block (ESPB), given after inguinal hernia surgery, can improve recovery quality, reduce pain, and help people get back to their daily activities sooner. About 60 adults having hernia repair will be randomly assigned to receive the block or standard pain care. Researchers will measure recovery scores, pain levels, and how long it takes to return to normal life up to 30 days after surgery.

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

Apr 2026

Finished

Jul 2026

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: 1. Patients aged between 18 and 65 years 2. Patients scheduled to undergo open IHT surgery under spinal anesthesia (unilateral) 3. Both male and female patients Exclusion Criteria: 1. Patients with coagulation disorders 2. Patients with chronic opioid use 3. Patients who develop intraoperative complications 4. Patients with a preoperative Numeric Rating Scale (NRS) pain score ≥4 5. Patients with a history of revision (recurrent) surgery 6. Patients unable to communicate for any reason 7. Patients who decline 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 Erector spinae plane block 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.

Erector spinae plane block Inguinal hernia unilateral Numeric rating scale Quality of recovery (qor-15) Return to daily activity

Contacts and locations

Locations

  • Muğla Training and Research Hospital

    Menteşe, Muğla, 48000, Turkey (Türkiye)

  • Sanliurfa Education and Research Hospital

    Sanliurfa, Eyyübiye, 63040, Turkey (Türkiye)

More trials for these conditions

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