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Could a 'Shoulder Pacemaker' boost recovery after joint replacement?

NCT ID NCT06501859

Symptom relief Sponsor: University of Utah 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether a device called the Shoulder Pacemaker can help people recover better after reverse shoulder replacement surgery. About 100 adults aged 18 to 80 will either receive standard physical therapy or therapy plus the device three times a week for three months. The goal is to see if the device reduces pain and improves shoulder function.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Shoulder Pacemaker device
What this could lead to
If it works, this device could offer a non-invasive way to improve recovery and reduce pain after shoulder replacement surgery.
What could go wrong
This is a small, early-stage study with only 100 participants. The device may not provide significant benefits over standard therapy, and results may not apply to all patients.

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.

Started

Aug 2023

Expected to finish

Jul 2027

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.

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 indicated for primary reverse shoulder arthroplasty * Surgery at University of Utah Facilities * Patients between the ages 18-80. Exclusion Criteria: * Prior ipsilateral shoulder arthroplasty * Inability or unwillingness to participate in the rehabilitation protocol * Prior cardiac pacemaker or spinal cord stimulator * Age over 80 * History of periscapular surgery * History of ipsilateral neurologic injury * Prisoners * Patients requiring prolonged immobilization deviating from standard protocol * Patients who have an implantable medical device or other electrical device.

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Conditions

The condition(s) this trial relates to.

Pain Shoulder Injuries

As listed by the trial registrant

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

Shoulder injuries

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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 Utah Orthopedics

    Salt Lake City, Utah, 84108, United States

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