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NCT07410650

Subscapularis-Sparing Total Shoulder Arthroplasty

Enrolling by Invitation
Not specifiedAges 18–90Observational
University of Utah
~50 participants
Updated 2026-02-13 on ClinicalTrials.gov
What's tested:Subscapularis-Sparing Total Shoulder Arthroplasty

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) Score
Measured over Pre-operative
+14 more outcomes measured

Conditions

Total Shoulder Arthroplasty

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NCT07410650

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Utah Orthopedics

    Salt Lake City, Utahno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Peter Chalmers, M.D. · PRINCIPAL_INVESTIGATOR · University of Utah Orthopaedics

Who to contact

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

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Eligibility criteria

Inclusion

Patients undergoing subscapularis-sparing anatomic total shoulder arthroplasty by the principal investigator at the University of Utah.

Exclusion

Patients unwilling to consent and comply with study procedures (i.e. follow up visits).
Patients under the age of 18.
Patients with contraindications to an anatomic total shoulder arthroplasty such as active infection, insufficient glenoid bone, damage to the rotator cuff, or a history of instability.
Patients with known prior shoulder arthroplasty.
Patients unable to undergo a magnetic resonance imaging study.

What this trial measures

  • Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) ScorePre-operative

    Shoulder specific scoring system out of 100. A patient-reported score with visual analog scale for pain and functional subscales ranging from 0 (worse pain and function loss) to 50 (no pain and excellent function). Both scores are summed for a maximum score of 100.

  • Patient-reported outcome (Simple Shoulder Test (SST))Pre-operative

    There are 12 shoulder specific questions which the patient answers "yes" or "no". The questions ask about strength, function and range of motion. To score the test, divide the number of "yes" answers by the total number of questions answered and then multiply by 100. 0% is the worst score to 100% being the best score.

  • Patient-reported outcome (Visual Analogue Score (VAS))Pre-operative

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

  • Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) Score6-weeks post-operative

    Shoulder specific scoring system out of 100. A patient-reported score with visual analog scale for pain and functional subscales ranging from 0 (worse pain and function loss) to 50 (no pain and excellent function). Both scores are summed for a maximum score of 100.

  • Patient-reported outcome (Simple Shoulder Test (SST))6-weeks post-operative

    There are 12 shoulder specific questions which the patient answers "yes" or "no". The questions ask about strength, function and range of motion. To score the test, divide the number of "yes" answers by the total number of questions answered and then multiply by 100. 0% is the worst score to 100% being the best score.

  • Patient-reported outcome (Visual Analogue Score (VAS))6-weeks post-operative

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

  • Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) Score3-months post-operative

    Shoulder specific scoring system out of 100. A patient-reported score with visual analog scale for pain and functional subscales ranging from 0 (worse pain and function loss) to 50 (no pain and excellent function). Both scores are summed for a maximum score of 100.

  • Patient-reported outcome (Simple Shoulder Test (SST))3-months post-operative

    There are 12 shoulder specific questions which the patient answers "yes" or "no". The questions ask about strength, function and range of motion. To score the test, divide the number of "yes" answers by the total number of questions answered and then multiply by 100. 0% is the worst score to 100% being the best score.

  • Patient-reported outcome (Visual Analogue Score (VAS))3-months post-operative

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

  • Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) Score1-year post-operative

    Shoulder specific scoring system out of 100. A patient-reported score with visual analog scale for pain and functional subscales ranging from 0 (worse pain and function loss) to 50 (no pain and excellent function). Both scores are summed for a maximum score of 100.

  • Patient-reported outcome (Simple Shoulder Test (SST))1-year post-operative

    There are 12 shoulder specific questions which the patient answers "yes" or "no". The questions ask about strength, function and range of motion. To score the test, divide the number of "yes" answers by the total number of questions answered and then multiply by 100. 0% is the worst score to 100% being the best score.

  • Patient-reported outcome (Visual Analogue Score (VAS))1-year post-operative

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

  • Patient-reported outcome (American Shoulder and Elbow Surgeons (ASES) Score2-years post-operative

    Shoulder specific scoring system out of 100. A patient-reported score with visual analog scale for pain and functional subscales ranging from 0 (worse pain and function loss) to 50 (no pain and excellent function). Both scores are summed for a maximum score of 100.

  • Patient-reported outcome (Simple Shoulder Test (SST))2-years post-operative

    There are 12 shoulder specific questions which the patient answers "yes" or "no". The questions ask about strength, function and range of motion. To score the test, divide the number of "yes" answers by the total number of questions answered and then multiply by 100. 0% is the worst score to 100% being the best score.

  • Patient-reported outcome (Visual Analogue Score (VAS))2-years post-operative

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