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Registry of Arthrex Hand and Wrist Products

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 26, 2025 (before its estimated December 1, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Primary completion date: Jun 1, 2024 to Dec 1, 2025v6 Show 5 more changesShow less
    • Enrollment target: 600 to 650
    • Study sites: 4 to 5
    • Study completion date: Dec 1, 2024 to Dec 1, 2025
    • Eligibility criteria revised
    • Study description expanded, about 11 words
  2. Study sites: 3 to 4v5
  3. Study sites: 2 to 3v4
  4. Study sites: 1 to 2
    • Primary completion date: Jun 2024 to Jun 1, 2024
    • Study completion date: Dec 2024 to Dec 1, 2024
    v3
  5. Enrollment target: 50 to 600v2 Show 4 more changesShow less
    • Start date changed from estimate of Sep 2021 to Jul 20, 2021
    • Interventions: Arthrex DX SwiveLock (Device), Bio-Compression Screw (Device), Bio-Suture Tak (Device), FastTak Titanium (Device), Headless Compression… to Products listed in cohort description (Device)
    • Study description shortened, about 30 words
    • Study arms: 0 to 1
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
A Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products
Trial Details
NCT Number NCT05046600
Lead Sponsor Arthrex, Inc.
Conditions
(from sponsor)		 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 +2 more
Related terms Ankylosis
Enrollment 650 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov