Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:01 PM
Ignite Modification Date:
2025-12-24 @ 7:01 PM
NCT ID:
NCT07145957
Eligibility Criteria:
Inclusion Criteria: • Patients aged 40-80
* Undergoing primary RSA for glenohumeral osteoarthritis or rotator cuff arthropathy
* Must be able to read and speak English
* Willing and able to attend a monthly therapy session and perform exercises at home for a minimum of 6 weeks before surgery
* Willing and able to participate in postoperative monitoring for a minimum of 2 years
Exclusion Criteria:
* Patients under the age of 40 and over the age of 80.
* Diagnosis of septic shoulder, fracture, or fracture sequelae, or tumor pathology of the ipsilateral shoulder
* Pre-existing hand, wrist, or elbow pathology that limits elbow flexion or extension, or forearm pronation or supination
* Planned to undergo synchronous procedure of the involved extremity (e.g., synchronous RSA and carpal tunnel release)
* Tendon transfer (e.g., Latissimus dorsi transfer) performed intraoperatively
* Patients without access to phone or email communication for at least 2 years after treatment
* Revision shoulder arthroplasty
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
40 Years
Maximum Age:
80 Years
Study:
NCT07145957
Study Brief:
Protocol Section:
NCT07145957