TerminatedNot Applicable

Measurement of Arch Motion After Bunion Surgery

Stopped: Surgeons chose not to provide patients for testing

United States2 participantsStarted 2014-02

Plain-language summary

This study is an observational "change from baseline" outcome measures design. Data is collected for the sake of evaluating treatment (fusion surgery) performed as standard medical care, but the investigator does not assign specific interventions to any participants in this study.

Who can participate

Age range18 Years – 80 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age 18 or older. * Women. * Able to comprehend the risks associated with the study. * Able to complete the paperwork required for enrollment. * Able to walk without assistance of another individual. Exclusion Criteria: * Pregnancy * History of great toe, forefoot or arch surgery, or severe traumatic injury. * Reduced ankle or great toe motion that impairs the ability to walk. * Observed evidence of foot deformity other than bunion. * Insensate to skin sensation testing which could indicate neuropathy.

What they're measuring

Fluoroscopy Examination of the Foot.

Timeframe: Change in Outcome Measurement [presurgery (baseline) and again 6 months postsurgery]

Trial details

NCT IDNCT02074748

SponsorUniversity of Minnesota

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2015-12

View on ClinicalTrials.gov More Hallux Valgus trials