Clinical Evaluation of Direct Manufactured Prosthetic Sockets

Completed · Phase 2

Conditions studied: Amputation

In brief

The purpose of this study is to evaluate a new prosthetic socket construction technique in order to improve the quality of care to lower extremity amputees.

Key facts

Study ID

NCT01155024

Run by

Ohio Willow Wood

People needed

10

Starts

2010-09-01

Expected to finish

2011-09-01

Last updated by the study team

2012-01-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be a lower extremity amputee longer than one year
• Be a consenting adult (at least 18 years or age or older)
• Albe to ambulate in current prosthesis without an aid (can, crutches or walker) for 30 minutes without rest
• Currently using a liner with prosthesis
• Be available during regular business hours for appointments

You may not qualify if…

• An inability to give informed consent
• Presence of any sores, lacerations or rashes on the residual limb
• Impaired contra lateral foot
• Poor distal sensation

Where it is running

• Ohio Willow Wood — Mount Sterling, Ohio, United States

Full record on ClinicalTrials.gov

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