NCT04694001

Evaluation of the Use of the Atalante Exoskeleton in Patients Presenting an Hemiplegia Due to Cerebrovascular Accident

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Wandercraft · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The INSPIRE study is interventional, European, prospective, open, multicentric, each patient being his/her own control. It is conducted to assess the safety and performance of the Atalante exoskeleton system in patients presenting an hemiplegia due to cerebrovascular accident. The primary endpoint is defined by the reported adverse events. The study will include 40 patients and takes place in six rehabilitation centers (4 in France, 1 in Luxembourg, 1 in Belgium).

Conditions

• Stroke
• Stroke, Acute
• Stroke, Subacute
• Chronic Stroke

Interventions

Type	Name	Description
DEVICE	Use of the Atalante exoskeleton	A session includes stand-up, walks, exercises with or without the assistance of the exoskeleton, rotation, side and back step, squat and sitting.

Timeline

• Start date: 2021-04-12
• Primary completion: 2022-03-28
• Completion: 2022-03-28
• First posted: 2021-01-05
• Last updated: 2022-04-27

Locations

6 sites across 3 countries: Belgium, France, Luxembourg