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Clinical Trials/NCT06284005
NCT06284005
Completed
Not Applicable

Multicentre Interventional Pilot Study on the Evaluation of the Functionality, Safety and Reliability of a New Robotic Prosthesis for the Lower Limb at the Transfemoral Level

Fondazione Don Carlo Gnocchi Onlus1 site in 1 country4 target enrollmentJuly 27, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Amputation
Sponsor
Fondazione Don Carlo Gnocchi Onlus
Enrollment
4
Locations
1
Primary Endpoint
ad hoc check-list Adverse Event
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this multicenter interventional pilot is to verify the functionality of a prosthesis for trans-femoral amputees.

The main question it aims to answer are:

  • Is to verify the technical functionality, safety and reliability of the propulsive lower limb prosthesis prototype, with active ankle, so as to provide indications regarding the technical and functional developments to be implemented in the finalization of the device.
  • Provide an indication of the functional effectiveness of the device and its satisfaction by patients.

Participants will perform:

  • walking tests inside parallel bars on flat and/or inclined terrain;
  • walking tests on treadmill;
  • stair climbing/descent tests.
Registry
clinicaltrials.gov
Start Date
July 27, 2020
End Date
December 22, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Claudio Macchi

Full Professor

Fondazione Don Carlo Gnocchi Onlus

Eligibility Criteria

Inclusion Criteria

  • trans femoural amputation
  • Medicare Functional Classification Levels k3-k4
  • expert prosthesis wearer (more than one year)
  • electronic knee prostheses user
  • energy-release prosthetic foot user

Exclusion Criteria

  • Relevant medical comorbidities
  • heart device wearers (PMK or AICD)
  • cognitive impairment
  • anxious or depressed illness

Outcomes

Primary Outcomes

ad hoc check-list Adverse Event

Time Frame: day 5

questionnaire that evaluate the device feasibility of the prosthesis and description of any adverse events.

Study Sites (1)

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