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Clinical Trial Summary

The prospective, post-market, single-center clinical study will include 45 subjects who are candidates for surgery using the Arthrex QuickFix Small Staple for Akin osteotomy to correct hallux valgus interphalangeus. The purpose of the study is to evaluate the continued safety and effectiveness of the device. Device-related adverse events as well as patient reported outcomes (VAS, FFI, FAAM, VR-12) will be collected up to 1 year postoperative.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04776356
Study type Observational [Patient Registry]
Source Arthrex GmbH
Contact
Status Terminated
Phase
Start date May 25, 2021
Completion date June 29, 2023

See also
  Status Clinical Trial Phase
Completed NCT04284618 - Off Axis View Radiographs Assessing Hallux Valgus Interphalangeus in Hallux Valgus Deformity