prosthetic suspension system
Not Applicable
- Conditions
- ower limb amputation.Amputation at level between knee and ankle
- Registration Number
- IRCT2014012816395N1
- Lead Sponsor
- M/MOHE/HIR grant (project no: D000014-16001)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
The inclusion criteria for the study consisted of person with trans-tibial amputation, walking without walking aids, steady limb volume during the previous year, pain- and ulcer-free stump, and stump length of more than 11 cm.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ambulation. Timepoint: 4 weeks after use. Method of measurement: kinematic & kinetic gait analysis.
- Secondary Outcome Measures
Name Time Method Interface pressure. Timepoint: 4 weeks after use. Method of measurement: Pressure mapping.