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NCT05116722

Shoulder Pacemaker for Scapular Dyskinesia

Enrolling by Invitation
NAAges 18–80InterventionalTreatment
University of Utah
~20 participants
Updated 2026-05-05 on ClinicalTrials.gov
What's tested:Shoulder Pacemaker

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Visual Analog Scale (VAS) pain
Measured over Beginning of the study prior to initiating use of the pacemaker
+3 more outcomes measured

Conditions

Scapular Dyskinesis
Posterior Shoulder Instability

Where it's being run

1 sites across 1 states
Utah1

Study leadership

  • Robert Z Tashjian, MD · PRINCIPAL_INVESTIGATOR · University of Utah Orthopaedics

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Scapular Dyskinesis
Posterior Shoulder Instability

Exclusion

Rotator Cuff Tearing
Shoulder Arthritis
Patients with implantable electrical/electronic devices
If participants are using wearable electrical medical devices, such as glucose sensors or infusion pumps, these devices will be turned off or the participants will be excluded from the study.

What this trial measures

  • Visual Analog Scale (VAS) painBeginning of the study prior to initiating use of the pacemaker

    VAS pain score (0 no pain - 10 severe pain)

  • Visual Analog Scale (VAS) pain3-months

    VAS pain score (0 no pain - 10 severe pain)

  • Visual Analog Scale (VAS) pain6-months

    VAS pain score (0 no pain - 10 severe pain)

  • Visual Analog Scale (VAS) pain12-months

    VAS pain score (0 no pain - 10 severe pain)