Clinical Trials Directory

Trials / Completed

CompletedNCT04187209

Evaluation of the Use of the Atalante System in Patients Presenting a Non-traumatic Hemiplegia in Acute-subacute Phase (15 Days to 6 Months).

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

Summary

The SPIRIT study is interventional, national, 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 a non-traumatic acute-subacute hemiplegia. The primary endpoint is defined by the patient's ability to perform the 10 MWT with the Atalante system. The study will include at least 12 patients and takes place in three french rehabilitation centers.

Conditions

Interventions

TypeNameDescription
DEVICEUse of the Atalante exoskeletonA session includes a stand-up, walks over a distance of 10 meters, exercises with or without the assistance of the exoskeleton, U-turns and a sitting.

Timeline

Start date
2019-09-11
Primary completion
2021-01-13
Completion
2021-01-13
First posted
2019-12-05
Last updated
2024-09-26

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT04187209. Inclusion in this directory is not an endorsement.