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ENROLLING BY INVITATION
NCT07898098
NA

Early Rehabilitation After Transfemoral Amputation in Moderately Active Patients Using the Avior Knee

Sponsor: Median

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to compare microprocessor-controlled knee prostheses in early rehabilitation in amputees with transfemoral amputations and low mobility (K I-II). The main question it aims to answer is: * Does the Avior knee prosthesis in early rehabilitation improve the mobility and well-being of the patients? * Is the Avior knee prothesis suitable for use in early rehabilitation? * Is the Avior knee prothesis suitable for use of amputees with low mobility (K I-II? Researchers will compare the Avior knee prothesis to the Kenevo knee prothesis to see if the preious results are achieved or surpassed. Participants will: * wear the knee protheses to be tested for 6 months * complete mobility tests during their 6 weeks stay at the rehabilitation facility (every 3 weeks --\> total: 3 times) * fill out questionairs concerning their mobilty and pain perception

Official title: "Comparison of Microprocessor-controlled Knee Prostheses in Early Rehabilitation Following Transfemoral Amputation and Low Mobility (I-II) - a Non-inferiority Study"

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

33

Start Date

2026-07-07

Completion Date

2027-07

Last Updated

2026-10-27

Healthy Volunteers

No

Interventions

DEVICE

knee prothesis - Avior

Usage of the Avior knee prothesis for 6 month during the interim period

DEVICE

knee prothesis - Kenevo

Usage of Kenevo knee prothesis for the duration of 6 months during the interim period

Locations (1)

MEDIAN Reha-Zentrum Wiesbaden Sonnenberg

Wiesbaden, Hesse, Germany