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Evaluation of Safety and Performance of the Atalante System With Patients With Lower Limb Paralysis

NCT04110561 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2019-10-07

No results posted yet for this study

Summary

The study is a prospective, open, bicentric and observational study. It is conducted to assess the safety and performance of the Atalante exoskeleton system with patients with lower limb paralysis.

The principal objective is to assess the performance of the Atalante system in performing ambulatory functions with motor complete SCI patients characterized by the success rate in performing a 10mWT at the last session of training with the Atalante system.

Conditions

  • Spinal Cord Injuries
  • Paraplegia
  • Paralysis, Lower Limbs
  • Lower Extremity
  • Robotics

Interventions

DEVICE

Use of the Atalante exoskeleton

A session basically includes a stand up, walks over a distance of 10 meters, exercises, U-turns and a sitting

Sponsors & Collaborators

  • Wandercraft

    lead INDUSTRY

Principal Investigators

  • Jacques Kerdraon, Dr · Centre mutualiste de Rééducation et de Réadaptation de Kerpape

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-05
Primary Completion
2018-11-16
Completion
2018-11-16

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04110561 on ClinicalTrials.gov