Registry of Arthrex Hand and Wrist Products

Conditions

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

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Accepted

Interventions

• Products listed in cohort description — DEVICE
  Depending on approved indication per product

Study Details

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

Key Dates

Start date

Jul 20, 2021

Status verified

Jun 2025

Primary completion

Dec 1, 2025

Completion

Dec 1, 2025

Study Design

Enrollment

650 participants (estimated)

Arms

• Arm: All Products listed in Descriptions
  Biocomposite™ or PEEK PushLock, DX SwiveLock SL, Headless Compression Screws, Tenodesis Screw (Biocomposite and PEEK), Corkscrew® Titanium (Nano and Micro-Corkscrew), DynaNite Nitinol Staples KreuLock Screws

Primary Outcome Measure

To assess a change in Visual Analogue Scale (VAS) survey [ Time Frame: Preoperatively, 3 months, 6 months and 12 months postoperatively ]

Central Contacts

• Justin F Moss, DHSc,CCRP
  7705844972
  [email protected]

Locations (5)

Find similar trials in Phoenix, AZ

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• Evaluating the Effectiveness of Remote Monitoring for Post-Operative Management of Distal Radius Fractures
  Enrolling By Invitation · University of Missouri-Columbia · Columbia, Missouri