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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00584103
Date of registration: 20/12/2007
Primary sponsor: University of Oklahoma
Public title: Evaluation of Upper Extremity Prosthesis
Scientific title: Evaluation of an Inexpensive Upper Extremity Prosthesis
Date of first enrolment: January 2007
Target sample size: 10
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00584103
Study type:  Interventional
Study design:  Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment  
Countries of recruitment
United States
Contacts
Name:   Daniel Hunt, B.S., C.O.
Address: 
Telephone:
Email:
Affiliation:  University of Oklahoma Health Sciences Center Department of Orthopedic Surgery & Rehabilitation, Division of Orthotics & Prosthetics
Key inclusion & exclusion criteria

Inclusion Criteria:

- Adult patients with unilateral transradial amputation

- Neurologically intact

- At least 6 months post amputation surgery

- Skin integrity intact without ulceration

Exclusion Criteria:

- Bilateral upper extremity amputees

- Patients that are insensate

- Patients with poor skin integrity

- Patients whose residual limb lengths preclude them from using the transradial
prosthesis that is being evaluated



Age minimum: 18 Years
Age maximum: 89 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Transradial Amputation
Intervention(s)
Device: Beta P prosthesis
Primary Outcome(s)
correct application and maintenance of position of device [Time Frame: 1 day -- time it takes to take measurements and make observations]
Secondary Outcome(s)
Secondary ID(s)
13099
ORTHDH 07
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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