RECRUITING

Registry of Arthrex Hand and Wrist Products

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

A Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products

Official Title

Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products

Quick Facts

Study Start:2021-07-20
Study Completion:2024-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05046600

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Subject requires surgery using Arthrex hand and wrist implants included in the registry.
  2. 2. Subject is 18 years of age or over.
  3. 3. Subject is not considered a vulnerable subject (i.e. child, pregnant, nursing, prisoner, or ward of the state).
  4. 4. Subject signed informed consent and is willing and able to comply with all study requirements.
  1. 1. Insufficient quantity or quality of bone.
  2. 2. Blood supply limitations and previous infections, which may retard healing.
  3. 3. Foreign-body sensitivity or foreign-body reactions.
  4. 4. Any active infection or blood supply limitations.
  5. 5. Conditions that tend to limit the patient's ability or willingness to restrict activities or follow directions during the healing period.
  6. 6. Subjects that are skeletally immature. -

Contacts and Locations

Study Contact

Justin F Moss, DHSc,CCRP
CONTACT
7705844972
justin.moss@arthrex.com

Study Locations (Sites)

MORE Foundation
Phoenix, Arizona, 85023
United States
University of Iowa
Iowa City, Iowa, 52242
United States
Duke University
Durham, North Carolina, 27705
United States
West Virginia University
Morgantown, West Virginia, 26501
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 Date2021-07-20
Study Completion Date2024-12-01

Study Record Updates

Study Start Date2021-07-20
Study Completion Date2024-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Ulnar/Radial Collateral Ligament Reconstruction
  • Ligament Repair or Reconstruction
  • Small Bone Fragments and Arthrodesis
  • Scapholunate Ligament Reconstruction
  • Carpal Fusion (Arthrodesis) of the Hand
  • Digital Tendon Transfers
  • Carpometacarpal Joint Arthroplasty