Rotator Cuff Tear Clinical Trial
Official title:
Healing After Arthroscopic Rotator Cuff Repair: A Prospective, Randomized Trial of Early Range of Motion Versus Immobilization
The purpose of this study is to better understand the influence of post-operative rehabilitation on the rate of tendon healing and clinical outcomes following arthroscopic repair of the rotator cuff. There are two schools of thought on what type of therapy program is most beneficial following surgical cuff repair. However there has been little data available to compare them. Therefore, the investigators would like to compare these two standard plans of care so that the investigators may better define the safety and efficacy of early mobilization of the shoulder versus keeping the shoulder immobilized following surgical management.
Status | Completed |
Enrollment | 150 |
Est. completion date | August 2012 |
Est. primary completion date | August 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 40 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Full-thickness tears of the rotator cuff involving the supraspinatus that may or may not include the infraspinatus tendon (less than 25 mm anteroposterior dimension) 2. Arthroscopic double-row cuff repair Exclusion Criteria: 1. Acute rotator cuff tears less than 6 weeks from injury 2. Subscapularis tendon tears (full thickness) 3. Preoperative stiffness: loss of greater than 30 passive elevation and/or ER compared to the opposite shoulder 4. Inability to comply with postoperative rehabilitation protocols 5. Inflammatory disease 6. Prior surgery of the shoulder |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Washington University School of Medicine - Department of Orthopedics | St. Louis | Missouri |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | Barnes-Jewish Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical evaluation of Shoulder function and strength | 3 months, 6 months, 1 year and 2 years post op | No | |
Secondary | Evaluation of cuff repair integrity using Ultrasound at 1 year post op | 1 year post op | Yes |
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