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Clinical Trial Summary

In order to gather enough data for meaningful statistics, a multicenter register of all flexor tendon repairs was established with surgical, clinical and rehabilitation patient data. The controlled active motion (CAM) protocol was administered in all patients after surgery. The purpose was to (i) measure surgery and therapy outcomes in the three centers and (ii) evaluate potential influencing factors on outcomes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04312412
Study type Observational
Source University of Zurich
Contact Vera Beckmann-Fries
Phone +41 44 255 51 24
Email vera.beckmann-fries@usz.ch
Status Recruiting
Phase
Start date January 1, 2014
Completion date December 31, 2026

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