Clinical trial to compare walking of existing non-powered and bio-signal recognition robot artificial leg in patients who underwent lower leg amputation and peripheral nerve interface surgery who participated in the clinical study of smart lower extremity
Not Applicable
- Conditions
- Factors influencing health status and contact with health services
- Registration Number
- KCT0007791
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 6
Inclusion Criteria
1) Patients who have undergone below knee amputation and peripheral nerve interface surgery who participated in previous year's clinical trial
2) Patients weighing less than 45kg to 100 kg
3) Patients with K-level 1 or higher during screening
4) Patients who use non-powered lower extremities artificial leg
Exclusion Criteria
1) Patients who weigh less than 45kg or weigh more than 100kg
2) Patients with skin problems in the robot prosthetic leg contact area
3) Patients with cognitive dysfunction
4) Patients with accompanying diseases or health conditions affecting the study;
5) Patients with visual disorders who have difficulty participating in the virtual reality amputation rehabilitation unit
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Gait evaluation
- Secondary Outcome Measures
Name Time Method Pain evaluation