Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05046600

Registry of Arthrex Hand and Wrist Products

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

Status
Recruiting
Phase
—
Study type
Observational
Enrollment
650 (estimated)
Sponsor
Arthrex, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

The objective of the registry is to evaluate the continued safety and effectiveness of the Arthrex hand and wrist products including the Biocomposite or PEEK PushLock® Anchors for ulnar/radial collateral ligament reconstruction; and/or the DX SwiveLock® SL Anchors (3.5 x 8.5mm) for ligament repair or reconstruction (e.g. scapholunate ligament reconstruction, ulnar/radial collateral ligament reconstruction, and carpometacarpal joint arthroplasty); and/or, the Headless Compression Screws for small bone fragments; and/or, the arthrodesis Tenodesis Screw (Biocomposite and PEEK), for ulnar collateral ligament reconstruction; and/or, the Corkscrew® Titanium Anchor (Micro Corkscrew® Anchor) for ulnar/radial collateral ligament reconstruction, digital tendon transfers (Nano Corkscrew® Anchor); and/or, the DynaNite® Nitinol Staples for carpal fusion (arthrodesis) of the hand; and/or, the KreuLock™ Screws for Distal Radius

Conditions

Interventions

TypeNameDescription
DEVICEProducts listed in cohort descriptionDepending on approved indication per product

Timeline

Start date
2021-07-20
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2021-09-16
Last updated
2025-06-26

Locations

5 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05046600. Inclusion in this directory is not an endorsement.