Total Shoulder Arthroplasty Multi-Center Registry

Description

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

Conditions

Shoulder Arthroplasty

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Study Overview

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Study Details

Study overview

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

Total Shoulder Arthroplasty Multi-Center Registry

Total Shoulder Arthroplasty Multi-Center Registry

Condition
Shoulder Arthroplasty
Intervention / Treatment

-

Contacts and Locations

Phoenix

University of Arizona/Banner Health, Phoenix, Arizona, United States, 85006

Phoenix

Banner Medical Group, Phoenix, Arizona, United States, 85016

Scottsdale

Scottsdale, Arizona, United States,

Denver

Denver, Colorado, United States,

Farmington

University of Connecticut Health Center, Farmington, Connecticut, United States, 06030

Gulf Breeze

Andrews Research & Education Foundation, Gulf Breeze, Florida, United States, 32561

Ann Arbor

The University of Michigan, Ann Arbor, Michigan, United States, 48105

Grand Rapids

Grand Rapids, Michigan, United States,

Columbia

Columbia, Missouri, United States,

New York

The Rothman Institute, New York, New York, United States, 10022

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patient voluntarily consents to participate in the study and has the mental and physical ability to participate in the study, fill out subjective questionnaires, return for follow-up visits, and comply with prescribed post-operative physical therapy.
  • 2. Patient is between the ages of 18 and 100 years.
  • 3. The patient has a planned primary or revision implantation of an anatomic (hemi-arthroplasty or total arthroplasty) or a reverse shoulder prosthesis system manufactured by Arthrex.
  • 4. Patient has a standard of care preoperative CT taken within 6 months that has been submitted for Arthrex VIP (Virtual Implant Positioning) planning.
  • 1. Patient has known intentions, obligations, or co-morbidity that would inhibit them from participating in the study.

Ages Eligible for Study

18 Years to 100 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Arthrex, Inc.,

Study Record Dates

2027-11-10