A Study in the Comparison of Gait Non-powered and Robot artificial leg in Patients with Above knee amputation

Comparative Clinical Study on Gait Between Conventional Non-Powered Transfemoral Prosthesis and Smart Electronically Controlled Transfemoral Prosthesis in Patients with Transfemoral Amputation

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009945

Enrollment

Registered

2024-11-22

Start date

2024-10-15

Completion date

Unknown

Last updated

2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : This clinical trial involves conducting basic examinations and K-Level assessments for patients who meet the inclusion/exclusion criteria. The K-Level is used as an index for evaluati

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Subjects who have undergone femoral amputation or peripheral nerve interface writing in the last 50 years 2) Patients with a body weight within the range of 45kg to 100kg 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

Exclusion criteria: 1) Patients with a body weight less than 45kg or exceeding 100kg 2) Patients with skin disorders on the contact area of the robotic prosthesis 3) Patients with cognitive impairments 4) Patients with coexisting diseases or health conditions that may impact the research(e.g.stroke, pacemaker placement, severe ischemicheart disease, etc)

Design outcomes

Primary

Measure	Time frame
Gait evaluation	—

Secondary

Measure	Time frame
pain evaluation	—

Countries

Korea, Republic of

Contacts

Public ContactJuhee Hwang

Asan Medical Center

juheex301@gmail.com+82-2-2045-4291

Outcome results