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Which nerve block eases heart surgery pain better? new study aims to find out.

NCT ID NCT07287761

Symptom relief Sponsor: Ankara 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 01, 2026 · Updated 2 times

Summary

This study compares two types of nerve blocks (ESPB and SPSIPB) to manage pain after heart bypass surgery. About 60 adults aged 18-80 having planned bypass surgery will take part. The goal is to see which block reduces the need for painkillers and improves comfort 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.

Participants

55 people

The number who actually took part.

Started

Jun 2025

Finished

Feb 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.

Who is studied

The study population consists of adult patients (18 to 80 years) classified as ASA Physical Status Class II or III, who are scheduled to undergo elective Coronary Artery Bypass Grafting (CABG) requiring median sternotomy at the University of Health Sciences Ankara Training and Research Hospital.

Ages

18 to 80 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 elective Coronary Artery Bypass Grafting (CABG) via median sternotomy. * Age between 18 and 80 years. * Classification of American Society of Anesthesiologists (ASA) Physical Status Class II or III. * Patients who provide written and verbal informed consent to participate in the study. Exclusion Criteria: * Patients who do not provide consent. * Age older than 80 years or ASA Physical Status Class \> III. * Patients who do not understand the Numerical Rating Scale (NRS) or have communication difficulties. * Patients with a known history of coagulation disorders or bleeding disorders. * Patients with skin infection at the site of peripheral nerve block application. * Patients with Morbid Obesity (Body Mass Index BMI\>35 kg/m2). * Patients with chronic pain, opioid or substance dependence, or who use chronic analgesics. * Patients with known allergy to local anesthetics. * Patients with liver or kidney function disorders. * Patients with a history of previous median sternotomy operation. * Patients undergoing emergency surgery.

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Conditions

The condition(s) this trial relates to.

coronary artery disorder myocardial ischemia Pain, Postoperative

As listed by the trial registrant

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

Coronary artery bypass graft (CABG) Postoperative pain after thoracic surgery

Contacts and locations

Locations

  • Ankara Training and Research Hospital

    Ankara, Altındag, 06230, Turkey (Türkiye)

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