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New nerve block combo aims to slash opioid use after heart surgery

NCT ID NCT07622823

Symptom relief Sponsor: Antalya Health Sciences University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether combining two types of nerve blocks can help people who have heart surgery use fewer strong painkillers (opioids) and recover better. About 90 adults having planned heart surgery will receive one of two nerve block combinations. Researchers will measure how much pain medicine they need, their recovery quality, and if they develop long-term pain.

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

About 90 people

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

Started

Jun 2026

Expected to finish

Dec 2026

An estimate. End dates often move.

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.

Who is studied

It is planned to include ASA score I-IIII adult patients who are scheduled to elective cardiac surgery

Ages

18 years and older

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: * elective cardiac surgery planned * over 18 years, adult * American Society of Anaesthesiology (ASA) score I-III Exclusion Criteria: * under 18 years of age, * ASA IV and above, * contraindications for the block application * history of cardiac surgery, * reoperated due to surgery-related complications after emergency surgery or postoperative elective surgery, * off-pump cardiac surgery or minimally invasive cardiac surgery * unable to be extubated in the intensive care unit at 24 hours postoperatively * history of chronic pain treatment * chronic alcoholism and substance abuse * declining to give written informed consent

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As listed by the trial registrant

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

Cardiovascular surgery Postoperative analgesia Regional anaesthesia

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

  • University of Health Sciences, Antalya Training and Research Hospital

    RECRUITING

    Antalya, Turkey (Türkiye)

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