TerminatedNot Applicable

Wright Foot & Ankle Post-Market Observational Study

Stopped: Due to COVID the enrollment into the study was delayed. Sponsor chose to collect clinical data via alternative methods.

United States, France, Germany119 participantsStarted 2020-01-22

Plain-language summary

WRIGHT FOOT \& ANKLE POST-MARKET OBSERVATIONAL STUDY, Multi-Year, Multi-Site, Multi-Device, Post-Market Observational Study, 10 sites, a minimum of 40 patients per device

Who can participate

Age range18 Years

SexALL

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: * Willing and able to consent to participate (written, informed consent); * Willing and able to attend/complete the requested follow-up visits; * Considered for treatment with one or more approved or cleared Wright Medical products included in this study Exclusion Criteria: * Subjects determined, by the investigator, to be an inappropriate candidate for the procedure indicated; * Unable to consent to participate (written, informed consent); * Unable to attend/complete the requested follow-up visits

What they're measuring

EuroQol (EQ-5D-5L).

Timeframe: 1 year

Trial details

NCT IDNCT04118894

SponsorStryker Trauma and Extremities

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2022-12-08

Results submitted2024-11-05

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