RECRUITING

Total Shoulder Arthroplasty Multi-Center Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Total Shoulder Arthroplasty Multi-Center Registry

Quick Facts

Study Start:2015-07-28
Study Completion:2027-11-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03511586

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.

Ages Eligible for Study:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 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. 2. Patient is between the ages of 18 and 100 years.
  3. 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. 4. Patient has a standard of care preoperative CT taken within 6 months that has been submitted for Arthrex VIP (Virtual Implant Positioning) planning.
  5. 1. Patient has known intentions, obligations, or co-morbidity that would inhibit them from participating in the study.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Kelly Ganz, BA, CCRC
CONTACT
1 (800) 933-7001
kelly.ganz@arthrex.com
Alicia Ruiz, MS, CCRP, CCRA
CONTACT
1 (800) 933-7001
alicia.ruiz@arthrex.com

Study Locations (Sites)

University of Arizona/Banner Health
Phoenix, Arizona, 85006
United States
Banner Medical Group
Phoenix, Arizona, 85016
United States
Scottsdale, Arizona
United States
Denver, Colorado
United States
University of Connecticut Health Center
Farmington, Connecticut, 06030
United States
Andrews Research & Education Foundation
Gulf Breeze, Florida, 32561
United States
The University of Michigan
Ann Arbor, Michigan, 48105
United States
Grand Rapids, Michigan
United States
Columbia, Missouri
United States
The Rothman Institute
New York, New York, 10022
United States
University of North Carolina
Chapel Hill, North Carolina, 27599
United States
Cleveland Shoulder Institute
Beachwood, Ohio, 44122
United States
Medford, Oregon
United States
The Hawkins Foundation
Greenville, South Carolina, 29615
United States
Germantown, Tennessee
United States
University of Virginia
Charlottesville, Virginia, 22903
United States
Virginia Beach, Virginia
United States

Collaborators and Investigators

Sponsor: Arthrex, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2015-07-28
Study Completion Date2027-11-10

Study Record Updates

Study Start Date2015-07-28
Study Completion Date2027-11-10

Terms related to this study

Additional Relevant MeSH Terms

  • Shoulder Arthroplasty