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
| Type | Name | Description |
|---|---|---|
| DEVICE | Use of the Atalante exoskeleton | A 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.