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Clinical Trial Summary

To gather prospective safety and effectiveness data for the C-Brace System following the standard of care.


Clinical Trial Description

The purpose of the C-Brace Prospective Registry is to gather prospective baseline and follow-up data to characterize the safety and effectiveness of the C Brace. Patients casted for C-Brace fitting and willing to provide informed consent at participating clinics will be enrolled in the registry. All patients will be followed in accordance with the standard of care for a C-Brace, which will include, at a minimum, baseline evaluation, fitting, patient training/therapy sessions, follow-up at 6 months, 12 months, 24 months and 36 months after the definitive fitting of the C-Brace. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04640584
Study type Observational [Patient Registry]
Source Otto Bock Healthcare Products GmbH
Contact Russell L Lundstrom, MS
Phone 512-806-2606
Email russ.lundstrom@ottobock.com
Status Recruiting
Phase
Start date April 2015
Completion date April 2026

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