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Rotator Cuff Injuries clinical trials

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NCT ID: NCT04673344 Enrolling by invitation - Rotator Cuff Tears Clinical Trials

Regeneten Patch vs Standard Care in Partial Thickness Rotator Cuff Repair

Start date: December 30, 2020
Phase: N/A
Study type: Interventional

Shoulder pain is a common complaint with the most common reason being tendinopathy and/or tearing of the rotator cuff. While many rotator cuff tears are often considered normal, age-related degenerative disorders, with either partial- or full-thickness rotator cuff tears evident in 4% of patients aged <40 years and in 54% of patients aged >60 years, once they become symptomatic and conservative management fails, they are typically repaired surgically. Data suggest that the incidence of surgery to repair and re-attach the cuff continues to rise. However, despite positive clinical results overall, reports of repair failure after surgery can range from 16%-94%, and of those that do fail, or fail to heal, generally do so within the first 3 to 6 months post-surgery. Given the aforementioned reported issues with the gold standard for the treatment of unresponsive and symptomatic partial or full rotator cuff tears (surgical repair), together with the invasiveness of this surgery and lengthy period of restricted activity, other means of treatment have been proposed. The REGENETEN scaffold/implant seeks to support new tendon growth and disrupt disease progression. This study seeks to investigate the outcome of surgical rotator cuff repair versus scaffold augmentation (using the REGENETEN scaffold) for symptomatic partial thickness rotator cuff tears.

NCT ID: NCT04278716 Enrolling by invitation - Clinical trials for Labral Tear, Glenoid

Return to Play Checklist

Start date: May 14, 2018
Phase:
Study type: Observational

This study will try to develop and determine objective and validated criteria for our athletes to safely return to sports after labral repair.

NCT ID: NCT01405781 Enrolling by invitation - Shoulder Pain Clinical Trials

Functional and Radiographic Outcomes After Shoulder Surgery

Start date: May 2011
Phase:
Study type: Observational

The objective of this study is twofold: First, to determine whether higher levels of pre-operative psychological distress predict worse outcomes after arthroscopic rotator cuff repair; second, to obtain functional outcomes (VAS pain, VAS satisfaction, VAS function, Simple Shoulder Test (SST) and American Shoulder and Elbow Surgeons (ASES) Score), physically examine and perform a radiographic analysis of patients at a minimum of 6 months after reverse total shoulder arthroplasty, total shoulder arthroplasty, arthroscopic scapulothoracic bursectomy, acromioclavicular joint reconstruction and arthroscopic rotator cuff repair.

NCT ID: NCT01193647 Enrolling by invitation - Clinical trials for Studying the Genetic Relationship of Rotator Cuff Tears

Genetic Factors Affecting Risks for Rotator Cuff Disease

Start date: July 2009
Phase:
Study type: Observational

This study will begin to evaluate the heritability of rotator cuff disease, and begin creation of a powerful resource for future genetic studies of rotator cuff disease.