Clinical Trials Logo

Clinical Trial Summary

The objective of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.


Clinical Trial Description

The study is a non-randomized multi-center prospective registry and subjects will be treated according to standard of care at each center. Subjects will be approached for participation in this study after they have made the decision to undergo a primary or revision shoulder arthroplasty procedure. The treating surgeon will obtain verbal consent from the patient for a research coordinator to screen for eligibility. Patients who meet all criteria will be offered enrollment into the study. The total enrollment goal is a minimum of 500 anatomic shoulder arthroplasty and 500 reverse shoulder arthroplasty subjects enrolled in the multi-center registry. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03511586
Study type Observational [Patient Registry]
Source Arthrex, Inc.
Contact Kelly Ganz, BA, CCRC
Phone 1 (800) 933-7001
Email kelly.ganz@arthrex.com
Status Recruiting
Phase
Start date July 28, 2015
Completion date November 10, 2027

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05965986 - Preoperative Rehabilitation and Education Program N/A
Completed NCT05020821 - Superior Trunk Block Catheter Versus Single-shot Superior Trunk Block With Intravenous Dexmedetomidine for Shoulder Arthroplasty N/A
Completed NCT05350319 - Prospective Low Dose CT for Total Shoulder Arthroplasty/Reverse Shoulder Arthroplasty
Terminated NCT03845894 - Interscalene Block With Liposomal Bupivacaine vs. Interscalene Block With Bupivacaine and Adjuvants Phase 4
Recruiting NCT05699031 - Shoulder Prosthesis Telerehab Care Trial N/A
Completed NCT04822610 - Comparison of Interscalene Block and Suprascapular With Axillary Block N/A
Terminated NCT03880955 - A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty (RSA) System
Terminated NCT03858517 - A Post-Market Clinical Evaluation of the ReUnion TSA System
Completed NCT04112407 - The Effect of Pretreatment for Propionibacterium Acnes on Surgical Site Burden in Shoulder Arthroplasty N/A
Recruiting NCT03268837 - Programmed Intermittent Bolus During Continuous Interscalene Nerve Block for Shoulder Arthroplasty N/A
Active, not recruiting NCT06281574 - What Are the Determinants for RTW After SA
Completed NCT05179941 - Subscapularis Indocyanine Green Perfusion Pilot Study N/A
Completed NCT03578237 - Cryoanalgesia to Prevent Acute and Chronic Pain Following Surgery: A Randomized, Double-Masked, Sham-Controlled Study N/A
Recruiting NCT00527839 - Hospital for Special Surgery Shoulder Arthroplasty Cohort