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

NCT05199246 · Institut de Myologie, France · Updated 16 April 2026

What is being tested
Lower-limb powered dermoskeleton
For
Muscular Dystrophies; Congenital Myopathy; Idiopathic Inflammatory Myopathies; Mitochondrial Myopathies; Glycogen Storage Disease
Kind of study
Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
Who can join
Ages 18 years to 70 years. About 50 people. The full rules are on the registry page.
Where
France
When
Starts or started 1 Dec 2021, ends 22 April 2025. Registered 20 Jan 2022.
Results
None posted yet.

In the researchers' words

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.
ClinicalTrials.gov, NCT05199246

Sites

  • Institute of MyologyParis, France