C-Brace Prospective Registry
A Prospective Registry of Patients Fitted With a Microprocessor-controlled Knee Ankle Foot Orthosis
Otto Bock Healthcare Products GmbH
250 participants
Apr 1, 2015
OBSERVATIONAL
Conditions
Summary
To gather prospective safety and effectiveness data for the C-Brace System following the standard of care.
Eligibility
Inclusion Criteria3
- 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 Criteria2
- Patient is geographically inaccessible to comply and participate in the registry.
- Patient has not been casted for a C-Brace fitting.
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Interventions
The C-Brace consists of individually fabricated thigh, calf and foot components. An ankle joint, unilateral or bilateral fitting, or an individual spring element connects the foot and calf components. The sensor system continuously measures the flexion of the knee joint and its angular acceleration. This allows the C-Brace to detect the user's current walking phase, so it can regulate the hydraulic resistances as well as control the flexion and extension of the knee joint.
Locations(76)
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NCT04640584