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Clinical Trial Summary

The purpose of this multicentric study is to assess the impact of C-BRACE on mobility, endurance, confidence, participation, satisfaction, psychosocial adjustment and quality of life in community ambulators using a Stance Control Orthosis.


Clinical Trial Description

During two months of inclusion period, the investigators invite all patients matching with inclusion criteria for an enrolment visit, collect written consent and record general patient information. The eCRF (electronic Case Report Form) assigns the enrolled patient into one group for the trial (C-BRACE/SCO or SCO/C-BRACE), in a randomized order. The assessments are performed after 2 month follow-up period with each orthosis with a minimal wash-out period of 2 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05332509
Study type Interventional
Source Otto Bock France SNC
Contact
Status Completed
Phase N/A
Start date April 19, 2022
Completion date April 17, 2023

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