NCT04196114

Study on Feasibility of Stimulation on the Lumbar Part of the Spinal Cord to Improve Mobility Recovery in Patients With Sub-acute Spinal Cord Injury

Study on Feasibility of Targeted Epidural Spinal Stimulation to Improve MObility Recovery in Patients With Sub-acute Spinal Cord Injury

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: Ecole Polytechnique Fédérale de Lausanne · Academic / Other
• Sex: All
• Age: 18 Years – 70 Years
• Healthy volunteers: Not accepted

Summary

The STIMO-2 study aims to investigate TESS-supported rehabilitation training in sub-acute spinal cord injury (\< 6 months post-injury). The primary endpoint of this study is to assess the safety and feasibility of TESS. The preliminary effectiveness of the therapy is the secondary study endpoint. The mobility recovery status of patients, who undergo TESS-supported rehabilitation, will be assessed at 12 months post SCI, compared to their predicted recovery expectations based on standard rehabilitation program

Conditions

• Spinal Cord Injury

Interventions

Type	Name	Description
DEVICE	STIMO-2 device implantation	Implantation of SCS lead in epidural space and implantation of neurostimulator in abdominal region

Timeline

• Start date: 2022-02-01
• Primary completion: 2023-03-31
• Completion: 2023-03-31
• First posted: 2019-12-12
• Last updated: 2023-10-05

Locations

1 site across 1 country: Switzerland