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Active clinical trials for "Rotator Cuff Tear Arthropathy"

Results 11-20 of 40

Massive Rotator Cuff Tear Reconstruction

Rotator Cuff Tear Arthropathy

To compare bridging reconstruction to superior capsular reconstruction using human dermal allograft augmentation for repair of massive rotator cuff tears.

Active13 enrollment criteria

Impact of Humeral Component Version on Outcomes Following RTSA

Rotator Cuff Tear Arthropathy

The proposed study is a prospective, single-blinded, randomized trial to investigate the impact of humeral component version on shoulder range of motion and patient reported functional outcomes following reverse total shoulder arthroplasty.

Active12 enrollment criteria

Clinical and Radiological Outcomes of Medacta Shoulder System FR

Primary OsteoarthritisSecondary Osteoarthritis5 more

This is a post-marketing surveillance on Medacta Shoulder System

Recruiting7 enrollment criteria

Exactech Shoulder Post Market Clinical Follow-up Study

Osteo Arthritis ShouldersOsteonecrosis7 more

The objective of this study is to collect and evaluate long-term clinical and radiographic outcomes data in order to better understand the safety and performance of the shoulder arthroplasty over time. This study will follow subjects long-term for a minimum of 10-years, without an early-term restriction on the amount of time they will be followed.

Recruiting23 enrollment criteria

Clinical and Radiological Outcomes of Medacta Shoulder System (BE)

Primary OsteoarthritisSecondary Osteoarthritis5 more

This is a post-market surveillance study on Medacta Shoulder System

Recruiting14 enrollment criteria

TESS V3 Modular Total Shoulder System PMCF

Osteoarthritis ShoulderRheumatoid Arthritis9 more

This is a multicenter, retrospective and prospective, non-controlled post market surveillance study. The objectives of this study are to confirm safety, performance and clinical benefits of the T.E.S.S.® Version 3 Anatomic and Reverse Modular Total shoulder prosthesis and its instrumentation.

Recruiting33 enrollment criteria

Follow-up Evaluating Clinical and Radiological Outcomes of Total Shoulder Arthroplasty With Permedica's...

Cuff Tear ArthropathyPrimary Osteoarthritis7 more

This observational study is conducted in order to evaluate the effectiveness of the primary total shoulder arthroplasty with the Permedica's MIRAI Modular Shoulder Prosthesis System on the general population of patients who are about to undergo this surgery for every indication. Patients requiring a revision shoulder arthroplasty will not be enrolled. The effectiveness will be evaluated in terms of recovery of shoulder function and stability of the prosthetic implant. The incidence of complications, adverse and serious adverse events will also be studied. Additional study aim is to evaluate a medium/long term survival of the prosthesis. The duration of the study per single subject is 5 years.

Recruiting20 enrollment criteria

Clinical and Radiological Outcomes of Medacta Shoulder System

Primary OsteoarthritisSecondary Osteoarthritis5 more

This is a post-marketing surveillance on Medacta Shoulder System

Recruiting7 enrollment criteria

Impact of Glenosphere Size on Range of Motion in Female Patients Undergoing Reverse Shoulder Arthroplasty...

Rotator Cuff Tear ArthropathyMassive Irreparable Rotator Cuff Tear

The purpose of this study is to perform a prospective randomized trial among female patients undergoing reverse shoulder arthroplasty (RSA) to determine if a larger glenosphere allows greater range of motion without an impact on complications.

Not yet recruiting10 enrollment criteria

Cutibacterium Acnes in Deep Tissues in Primary Spine and Shoulder Surgery

Rotator Cuff Tear ArthropathySpine Degeneration

Obtain deep tissue samples from patients undergoing primary prosthetic surgery of the shoulder and patients undergoing primary instrumented surgery of the spine. Patients will be randomized to receive benzoyl peroxide 3 days prior to surgery.

Not yet recruiting6 enrollment criteria

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