Clin2
NCT04715139Possibly a fitRecruiting

Testing safety of specific foot and ankle implants

Hyperpronated FootReconstruction Surgeries of the FootFixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/AnkleFixation of Small Bone Fragments of the Foot/AnkleLisfranc ArthrodesisMono or Bi-cortical Osteotomies in the ForefootFirst Metatarsophalangeal ArthrodesisAkin Osteotomy

Part of Bones, joints & muscles, Injuries & trauma clinical trials.

This study follows people who get certain Arthrex foot and ankle implants to check how safely they heal and work over time. It may help your care team by adding long-term information about these devices.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
700 people
Ages
2 years and older
Study type
Observational

Who can take part

  • You need surgery on your foot or ankle using specific Arthrex products included in their registry
  • You are 18 or older (unless the study includes a specific younger-group product called ProStop)
  • You (or a caregiver) can fill out study questionnaires on your own
  • You can return for all required follow-up visits during the healing period
  • You can sign consent (and assent if you’re a minor) and agree to follow all study instructions
  • You must meet the specific diagnosis/device rules for the exact Arthrex product you’re getting

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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