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Transfemoral Amputation clinical trials

View clinical trials related to Transfemoral Amputation.

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NCT ID: NCT06218238 Recruiting - Clinical trials for Transfemoral Amputation

A Biomechanical Evaluation of the Ossur Power Knee in Persons With Transfemoral Amputation

OPKTFA
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

Microprocessor-controlled knees (MPKs) do not typically utilize motors to power joint rotation, but they automatically adjust resistance or damping in the joint to improve swing- and/or stance-phase control as appropriate for the prosthesis user during gait. The Ossur Power Knee is the only commercially-available MPK that uses a motor to provide active power generation during walking and other activities. The purpose of this proposed investigation is to perform and compare biomechanical evaluations of the Power Knee and Ossur Rheo XC, a passive MPK, during walking and other activities by prosthesis users. Furthermore, mobility between male and female subjects will be compared to determine if there are differences in prosthetic knee usage on the basis of sex.

NCT ID: NCT06045468 Recruiting - Clinical trials for Transfemoral Amputation

Early Rehabilitation After Transfemoral Amputation in Moderately Active Patients

Start date: January 5, 2023
Phase: N/A
Study type: Interventional

Treatment and rehabilitation after transfemoral amputation represents a challenging medical field, involving intersectoral parties. Although treatment guidelines exists, their implementation is difficult. This study is conducted to evaluate the need to practice these guidelines in order to gain best benefits for the patients. Focus is set of early inpatient rehabilitation and the role of a microprocessor-controlled prothesis (Kenevo, Ottobock).

NCT ID: NCT05989243 Recruiting - Clinical trials for Transfemoral Amputation

Improving Socket Fit in Female and Male Veterans With Transtibial and Transfemoral Amputation

SocketFit
Start date: January 31, 2022
Phase:
Study type: Observational

The investigators do not yet know how a prosthetic socket with adjustable panels affects the performance of people with a lower limb amputation compared to a conventional prosthetic socket. The primary objective of this study is to compare an adjustable and conventional prosthetic socket and use this information to determine the optimal socket that would improve rehabilitation and function in people with lower limb amputation.

NCT ID: NCT05925712 Recruiting - Amputation Clinical Trials

Aerofit Post Market Investigation

Start date: June 6, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical investigation is to evaluate the clinical benefits of a ventilating suspension interface for individuals with transfemoral amputation. The main aim of the investigation will be to evaluate the clinical user-reported benefits to skin health from using a ventilating lower limb prosthetic suspension system and compare it to a non-ventilating suspension system.

NCT ID: NCT05831696 Recruiting - Clinical trials for Transfemoral Amputation

Metabolic Cost of Walking With Passive vs. Powered Prosthetic Knees Among Persons With Limb Loss

Start date: February 27, 2023
Phase: N/A
Study type: Interventional

The purpose of this industry-initiated research study is to test that a powered microprocessor controlled knee improves metabolic function during walking in level and sloped conditions as compared to the subject's physician prescribed prosthesis.

NCT ID: NCT05695911 Recruiting - Amputation Clinical Trials

Transfemoral Osseointegrated Prosthesis Limb-Load Symmetry Training

TOPLOAD
Start date: January 30, 2023
Phase: N/A
Study type: Interventional

This randomized controlled trial (n=25 enrolled, n=15 expected to complete) will 1) determine the feasibility of a 40-week limb-load biofeedback training intervention, 2) determine if there is an intervention signal of efficacy, and 3) identify functional movement priorities for people with transfemoral osseointegrated (OI) prostheses. A limb-load biofeedback training group (EXP (n=10)) will be compared to a standard of care attention-control group without limb-load biofeedback training (CTL (n=5)). Outcomes will be assessed at standard of care pre-habilitation end (Week 5), standard of care rehabilitation end (Week 24), and one year after OI Stage 2 surgery (Week 64).

NCT ID: NCT05662982 Recruiting - Clinical trials for Transfemoral Amputation

Sub-Ischial Socket for Transfemoral Amputation and Lower Mobility

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The objective of this trial is to assess use and benefits of the subischial socket for persons with transfemoral amputation and lower mobility levels. Specifically, the investigators will evaluate whether the subischial socket improves comfort, socket wear time, mobility, participation, quality of life and satisfaction with device than the standard-of-care ischial containment socket.