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C-Brace Prospective Registry

A Prospective Registry of Patients Fitted With a Microprocessor-controlled Knee Ankle Foot Orthosis

Who can join

All ages · All sexes

Inclusion Criteria:

* Patient has been evaluated and successfully tested with the Trial Tool, and has been casted for a C-Brace.
* Patient is able to communicate, provide feedback, understand and follow instructions during the course of the registry.
* Patient is willing to provide informed consent.

Exclusion Criteria:

* Patient is geographically inaccessible to comply and participate in the registry.
* Patient has not been casted for a C-Brace fitting.

About the study

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

What is being tested

• C-Brace (device)

Sponsor: Otto Bock Healthcare Products GmbH · Participants: 250 · Started: 2015-04

Contact the study team

• Russell L Lundstrom, MS · Phone: 512-806-2606
• Barbara Pobatschnig, MSc · Phone: +43 1 5233786-720

Official record on ClinicalTrials.gov — NCT04640584

Locations in the U.S.

Conditions

• Paresis

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.