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Clinical Trial Summary

The objective of this prospective study is to demonstrate accuracy of a limp detection model using a healthcare provider assessment as the non-reference standard.


Clinical Trial Description

The primary endpoint of the study is limp severity at the 4-6 week office visit. At 4-6 weeks (+/- 3 days) post-surgery, the healthcare team will assess the patient's limp severity by visual observation on a 3-point Likert scale (0=No limp, 1=Mild/Moderate or 2=Severe). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05693818
Study type Observational
Source Canary Medical
Contact Derek E. Coulter
Phone 18066816979
Email dcoulter@canarymedical.com
Status Recruiting
Phase
Start date January 31, 2023
Completion date May 15, 2024

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