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New nerve block could ease shoulder pain in stroke survivors

NCT ID NCT07302711

Symptom relief Sponsor: Marmara University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 30, 2026 · Updated 2 times

Summary

This study tests whether a special nerve block (PENG block) added to standard physical therapy can reduce shoulder pain and improve movement in people who have had a stroke. About 15 adults with stroke-related shoulder pain will receive the block or a placebo. The goal is to see if this approach helps with pain, range of motion, and quality of life.

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

15 people

The number who actually took part.

Started

Nov 2025

Finished

Jun 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.

Who is studied

Patients aged 18 to 85 years with post-stroke hemiplegic shoulder pain and limited shoulder joint range of motion will be recruited from the Pain Medicine and Physical Therapy Departments of Marmara University Pendik Training and Research Hospital. All participants will have experienced a stroke within the past year and will present with a Numeric Rating Scale (NRS) pain score of 4 or higher at baseline.

Ages

18 to 85 years

Sex

Anyone

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: * Age between 18 and 85 years Presence of hemiplegic shoulder pain with limited shoulder range of motion confirmed by clinical examination Numeric Rating Scale (NRS) pain score ≥ 4 Exclusion Criteria: * Severe deformity or pathology of the shoulder region Complex regional pain syndrome type I Presence of neglect syndrome Grade 4 glenohumeral joint degeneration Coagulopathy or bleeding disorders Fracture on the affected side Secondary pathology on MRI (malignancy or infection) History of allergic reaction to local anesthetic agents or dexamethasone Shoulder intervention or injection within the past 3 months Major psychiatric illness Refusal to participate in the study

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Conditions

The condition(s) this trial relates to.

hemiplegia Shoulder Pain

As listed by the trial registrant

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

Hemiplegia Shoulder pain

Contacts and locations

Locations

  • Marmara University

    Istanbul, Turkey, 34722, Turkey (Türkiye)

More trials for these conditions

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