Ulnar/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
Investigational drug(s) / intervention(s)
Products listed in cohort description
Products listed in cohort description: Depending on approved indication per product
Study summary
A Multi-Center, Prospective Registry to Evaluate the Continued Safety and Effectiveness of Hand and Wrist Products
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
1. Subject requires surgery using Arthrex hand and wrist implants included in the registry.
2. Subject is 18 years of age or over.
3. Subject is not considered a vulnerable subject (i.e. child, pregnant, nursing, prisoner, or ward of the state).
4. Subject signed informed consent and is willing and able to comply with all registry requirements
Exclusion Criteria:
1. Insufficient quantity or quality of bone.
2. Blood supply limitations and previous infections, which may retard healing.
3. Foreign-body sensitivity or foreign-body reactions.
4. Any active infection or blood supply limitations.
5. Conditions that tend to limit the patient's ability or willingness to restrict activities or follow directions during the healing period.
6. Subjects that are skeletally immature -
Primary outcome measure(s)
To assess a change in Visual Analogue Scale (VAS) survey — Preoperatively, 3 months, 6 months and 12 months postoperatively Patient reported pain scale 0-10 point scale (0 min,10 max)
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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