Actively Recruiting

Age: 18Years - 100Years
All Genders
ID03511586

Total Shoulder Arthroplasty Multi-Center Registry

Led by Arthrex, Inc. · Updated on 2025-08-11

2500

Participants Needed

24

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect clinical outcomes from patients undergoing anatomic or reverse total shoulder arthroplasty. It is a multi-center prospective registry focusing on patients who have decided to have either a primary or revision shoulder replacement surgery. The study is designed to gather data over time to better understand patient experiences and results after these procedures. Participants will receive shoulder arthroplasty treatment based on the usual care at each participating center. The study plans to enroll at least 500 subjects receiving anatomic shoulder replacements and 500 receiving reverse shoulder replacements. There is no randomization or experimental treatment involved; instead, the registry records outcomes following standard surgical procedures. During the study, patients will be asked to fill out questionnaires and attend follow-up visits to monitor their progress and recovery. Preoperative CT scans will be used for surgical planning, and participants will comply with prescribed physical therapy after surgery. The main outcome measured is the change in pain over a 10-year period, helping researchers understand long-term effects. Participants will be monitored throughout their recovery and beyond as part of the registry.

CONDITIONS

Brief Title

Total Shoulder Arthroplasty Multi-Center Registry

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient voluntarily consents and can participate in the study, complete questionnaires, attend follow-ups, and follow post-operative therapy
  • Patient is between 18 and 100 years old
  • Planned primary or revision implantation of an Arthrex anatomic or reverse shoulder prosthesis system
  • Standard preoperative CT scan within 6 months submitted for Arthrex VIP planning
Not Eligible

You will not qualify if you...

  • Patient has known intentions, obligations, or co-morbidities that would prevent participation in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Up to 2 weeks or until discharge

Participants undergo shoulder arthroplasty surgery and receive immediate post-operative care as part of their standard healthcare.

1 surgery visit and several post-operative visits

Post-operative Follow-up

Duration - Up to 10 years

Participants are followed for recovery and outcomes after surgery, including monitoring pain and function over time.

Regular follow-up visits over 10 years

Trial Site Locations

Total: 24 locations

1

University of Arizona/Banner Health

Phoenix, Arizona, United States, 85006

Actively Recruiting

2

Banner Medical Group

Phoenix, Arizona, United States, 85016

Actively Recruiting

3

Scottsdale, Arizona, United States

Actively Recruiting

4

Denver, Colorado, United States

Actively Recruiting

5

University of Connecticut Health Center

Farmington, Connecticut, United States, 06030

Terminated

6

Andrews Research & Education Foundation

Gulf Breeze, Florida, United States, 32561

Actively Recruiting

7

Advent Health Orlando

Orlando, Florida, United States

Actively Recruiting

8

NorthShore University Health System

Evanston, Illinois, United States, 60201

Withdrawn

9

The Trustees of Indiana University

Indianapolis, Indiana, United States, 46202

Actively Recruiting

10

The University of Michigan

Ann Arbor, Michigan, United States, 48105

Actively Recruiting

11

Grand Rapids, Michigan, United States

Terminated

12

Columbia, Missouri, United States

Terminated

13

The Rothman Institute

New York, New York, United States, 10022

Terminated

14

University of North Carolina

Chapel Hill, North Carolina, United States, 27599

Actively Recruiting

15

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States, 27157

Not Yet Recruiting

16

Cleveland Shoulder Institute

Beachwood, Ohio, United States, 44122

Active, Not Recruiting

17

Medford, Oregon, United States

Actively Recruiting

18

Rothman Orthopaedic Institute

Philadelphia, Pennsylvania, United States

Active, Not Recruiting

19

The Hawkins Foundation

Greenville, South Carolina, United States, 29615

Actively Recruiting

20

Germantown, Tennessee, United States

Actively Recruiting

21

University of Virginia

Charlottesville, Virginia, United States, 22903

Actively Recruiting

22

Virginia Beach, Virginia, United States

Actively Recruiting

23

Orthopädische Chirurgie München (OCM)

München, Germany, 81369

Actively Recruiting

24

Schulthess Klinik

Zurich, Switzerland, 8008

Actively Recruiting

Loading map...

Research Team

K

Kelly Ganz, BA, CCRC

A

Alicia Ruiz, MS, CCRP, CCRA

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Early Versus Delayed Rehabilitation After Reverse Total Shou...

Orthopedic Disorder

Actively Recruiting

1 location

Evaluating the Effects of Oral Tranexamic Acid on Short Term...

Shoulder Arthroplasty

Actively Recruiting

1 location

Prospective Evaluation of Clinical and Economic Outcomes of ...

Shoulder Arthroplasty

Actively Recruiting

2 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here