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New pain block comparison aims to reduce breathing risks in shoulder surgery recovery

NCT ID NCT07688395

Symptom relief Sponsor: Taksim Egitim ve Arastirma Hastanesi 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time

Summary

This study compares two ultrasound-guided nerve blocks—cervical erector spinae plane block and infraspinatus-teres minor interfascial plane block—for pain relief after shoulder arthroscopy. Both are designed to avoid the breathing complications sometimes caused by the standard interscalene block. The trial will measure pain scores and total painkiller use in the first 24 hours after surgery in adults aged 18 to 80.

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 proves better, it could offer safer, effective pain relief after shoulder surgery with fewer breathing risks than the current standard.
What could go wrong
This is a small, early-stage comparison study. Neither block may prove superior, and individual results may vary. Standard risks of nerve blocks still apply.

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 100 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Jul 2027

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 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: * Adults scheduled for elective shoulder arthroscopy * ASA I-II-III patients * Patients age between 18-80 Exclusion Criteria: * Patients with previously known allergy to local anesthetics. * Patients with insufficient pulmonary functions (Severe obstruction or restriction in Pulmonary Function Test) * Patients with ASA IV or higher * Patients who suffered from any complications related to anesthesia or surgery * Patients with additional body part injury * Pregnant or breastfeeding women

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As listed by the trial registrant

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

Shoulder arthroscopic surgery

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

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Contacts and locations

Locations

  • Taksim Educational and Research Hospital

    Istanbul, Beyoğlu, 34433, Turkey (Türkiye)

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