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Comparative Outcomes Assessment of the C-Leg With a New Knee Prosthesis

NCT01473992 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2023-12-12

Study results available
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Summary

The purpose of this study is to determine if transfemoral amputees of varied etiology will demonstrate increased function, safety and quality of life following accommodation with a new knee prosthesis as compared to their former C-Leg knee prosthesis.

Conditions

  • Other and Unspecified Complications of Amputation Stump

Interventions

DEVICE

Otto Bock C-Leg

Amputees' preferred prosthetic knee.

DEVICE

Otto Bock Genium

Study knee.

Sponsors & Collaborators

  • Otto Bock Healthcare

    collaborator INDUSTRY

  • Florida High Tech Corridor Council

    collaborator OTHER

  • Jason Highsmith

    lead OTHER

Principal Investigators

  • M. Jason Highsmith, PT,DPT,CP · University of South Florida

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • United States

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 NCT01473992 on ClinicalTrials.gov