Comparing the Outcome of Cemented All-Polyethylene Pegged vs. Keeled Components Through a Subscapularis Tenotomy or a Subscapularis Peel

Completed · Not applicable

Conditions studied: Arthropathy Shoulder, Shoulder Pain, Shoulder Osteoarthritis, Shoulder Arthritis, Shoulder Arthropathy Associated With Other Conditions, Necrosis of Bone, Arthritis, Inflammatory Arthritis

In brief

Participants who choose to participate in this study, will either have their tendon repaired to tendon, so-called tenotomy repair, or tendon repaired to bone, so-called peel repair.

Key facts

Study ID

NCT03735173

Run by

Mayo Clinic

People needed

4

Starts

2018-12-01

Expected to finish

2021-05-07

Last updated by the study team

2021-08-12

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects willing to sign the informed consent
• Male and female subjects ages 18 - 90 at the time of surgery
• Subjects indicated for an anatomic total shoulder arthroplasty (including primary glenohumeral osteoarthritis, avascular necrosis, and inflammatory arthritis)

You may not qualify if…

• Inability to comply with follow-up requirements
• Known or presumed substantial rotator cuff disorders
• Subjects with an active or suspected latent infection in or about the shoulder
• Subjects with instability (surgically or non-surgically addressed)
• Subjects presenting with posttraumatic avascular necrosis
• Need for glenoid bone grafting
• Pregnant subjects

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.