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Evaluation of a Novel Transfemoral Prosthetic Socket System

NCT01846845 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2013-07-01

No results posted yet for this study

Summary

The purpose of the study is to evaluate residual limb circulation and skin health associated with the use of a novel prosthetic transfemoral socket system. A conventional prosthesis will be compared to the novel transfemoral socket system.

Conditions

  • Lower Limb Amputation

Interventions

DEVICE

Conventional Prosthetic Transfemoral Socket System

Conventional transfemoral may include an ischial containment socket, a pin suspension socket, and/or suction suspension socket

DEVICE

Novel Prosthetic transfemoral socket system

Prosthetic socket that incorporates lower socket trim-lines and transfemoral vacuum suspension

Sponsors & Collaborators

  • Ohio State University

    collaborator OTHER

  • Ohio Willow Wood

    lead INDUSTRY

Principal Investigators

  • Gayle Gordillo, MD · Ohio State University

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2014-09-30
Completion
2014-09-30

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 NCT01846845 on ClinicalTrials.gov