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Registry of Arthrex Hand and Wrist Products

NCT05046600 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 650

Last updated 2025-06-26

No results posted yet for this study

Summary

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
  • Arthrodesis
  • Digital Tendon Transfer
  • Distal Radius Fracture Fixation

Interventions

DEVICE

Products listed in cohort description

Depending on approved indication per product

Sponsors & Collaborators

  • Arthrex, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-07-20
Primary Completion
2025-12-01
Completion
2025-12-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05046600 on ClinicalTrials.gov