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C-Brace Prospective Registry

NCT04640584 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2025-04-30

No results posted yet for this study

Summary

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

Conditions

  • Pareses
  • Lower Extremity

Interventions

DEVICE

C-Brace

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.

Sponsors & Collaborators

  • Otto Bock Healthcare Products GmbH

    lead INDUSTRY

Principal Investigators

  • Frank Braatz, Prof. · Private University of Applied Sciences

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • United States
  • Australia
  • Germany
  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04640584 on ClinicalTrials.gov