Health Trials

Registry of Arthrex Hand and Wrist Products

ConditionsUlnar/Radial Collateral Ligament ReconstructionLigament Repair or ReconstructionSmall Bone Fragments and ArthrodesisScapholunate Ligament ReconstructionCarpal Fusion (Arthrodesis) of the HandDigital Tendon TransfersCarpometacarpal Joint ArthroplastyArthrodesisDigital Tendon TransferDistal Radius Fracture Fixation
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorArthrex, Inc.

About this trial

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

Eligibility criteria

Qualifiers

Subject requires surgery using Arthrex hand and wrist implants included in the registry.

Subject is 18 years of age or over.

Subject is not considered a vulnerable subject (i.e. child, pregnant, nursing, prisoner, or ward of the state).

Subject signed informed consent and is willing and able to comply with all registry requirements

Disqualifiers

Insufficient quantity or quality of bone.

Blood supply limitations and previous infections, which may retard healing.

Foreign-body sensitivity or foreign-body reactions.

Any active infection or blood supply limitations.

Trial design

Treatments tested in this trial

  • Products listed in cohort description

Treatment groups

650 Participants
are divided into 1 treatment group

Sponsors and collaborators

Arthrex, Inc.

Lead sponsor

Source ClinicalTrials.gov