Registry of Arthrex Hand and Wrist Products

Description

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

Conditions

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

Talk to us

Study Overview

On this page

Study Details

Study overview

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

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

Registry of Arthrex Hand and Wrist Products

Condition
Ulnar/Radial Collateral Ligament Reconstruction
Intervention / Treatment

-

Contacts and Locations

Phoenix

MORE Foundation, Phoenix, Arizona, United States, 85023

Iowa City

University of Iowa, Iowa City, Iowa, United States, 52242

Durham

Duke University, Durham, North Carolina, United States, 27705

Morgantown

West Virginia University, Morgantown, West Virginia, United States, 26501

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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Arthrex, Inc.,

Study Record Dates

2024-12-01