Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT05199246
NA

Assessment of Safety and Acute Effects of a Lower-limb Powered Dermoskeleton in Patients With Neuromuscular Disorders

Sponsor: Institut de Myologie, France

View on ClinicalTrials.gov

Summary

The aims of the current study are as follow: i) Evaluate the safety, usability, and acute efficiency of a programmable ambulation exoskeleton (KeeogoTM Dermoskeleton System, B-Temia Inc., Quebec, Canada) in patients with neuromuscular disorders, ii) Elaborate recommendations regarding usability criteria for safe and efficient use the device in patients with neuromuscular disorders (e.g. type and severity of patient's functional deficits), iii) generate necessary data to foresee a future study involving a home use of the device and assessment of long-term benefits.

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2021-12-01

Completion Date

2025-04-22

Last Updated

2026-04-16

Healthy Volunteers

Yes

Interventions

DEVICE

Lower-limb powered dermoskeleton

Patients and healthy subjects will wear the movement assistance device to perform different standardised physical evaluations.

Locations (1)

Institute of Myology

Paris, France