Comparative Exploration Clinical Trial of Gait in Conventional Non-powered Thigh Prosthesis and Hip-Knee Combined Smart Robot Lower Limb Prosthesis
Not Applicable
Recruiting
- Conditions
- Injury, poisoning and certain other consequences of external causes
- Registration Number
- KCT0009095
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 4
Inclusion Criteria
1. Patients who have undergone femoral amputation surgery and/or peripheral nerve interface creation surgery in the last 50 years.
2. Patients with a body weight within the range of 45 kg to 100 kg.
3. Patients with a K-level of 1 or above during screening.
4. Patients using a conventional non-powered thigh prosthesis.
5. Patients aged 19 to 75 years.
Exclusion Criteria
Patients with a body weight less than 45 kg or exceeding 100 kg.
Patients with skin disorders on the contact area of the robotic prosthesis.
Patients with cognitive impairments.
Patients with coexisting diseases or health conditions that may impact the research (e.g., stroke, pacemaker placement, severe ischemic heart disease, etc.).
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Gait evaluation
- Secondary Outcome Measures
Name Time Method pain evaluation