| NCT06740006 | Retrospective Study on the WalkOn AFO in Children or Teenagers With Neurological Pathologies | Otto Bock France SNC | | - Age 4 - 17 yrs
- Level C1-S5
AIS - All
| Ended | 65 | | | Standing/walking/mobility | - Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST)
| 18 months | 03 September 2024 | 18 December 2024 | 1 | |
| NCT06740279 | Investigating the Upper Limb During the First 6 Months After Sustaining a Cervical Spinal Cord Injury, | Vastra Gotaland Region | | - Age ≥ 18 yrs
- Level C1-C7
AIS A, B, C, D- ≤ 1 months
| Recruiting soon | 210 | | | Arm/hand function | | 6 months | 07 January 2025 | 18 December 2024 | 0 | |
| NCT06511934 | Feasibility of the BrainGate2 Neural Interface System in Persons With Tetraplegia (BG-Tablet-01) | Massachusetts General Hospital | | - Age 18 - 80 yrs
- Level C1-T1
AIS - All
- have participated in the previous BrainGate2 trial (NCT00912041)
| Recruiting | 2 | NA | Technology | General health | - Adverse Events (AEs)
- Feasibility
| 1 year | 22 July 2024 | 22 July 2024 | 1 | |
| NCT06515223 | Improving Pelvic Rehabilitation Using Epidural Stimulation After Spinal Cord Injury | University College, London | | - Age ≥ 18 yrs
- Level C1-L5
AIS A, B, C, D- ≥ 1 years
- have neurogenic detrusor overactivity.
- Not have history of bladder sphincter surgery
| Recruiting | 20 | NA | Technology | Bladder health/function | - American Spinal Injury Association Impairment Scale (AIS): International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
- Bowel and bladder control
- European Quality of Life Five Dimension Five Level Scale (EQ-5D-5L)
- Neurogenic Bladder Symptom Score
- Neurogenic Bowel Dysfunction Score (NBD or NBDS)
- Penn Spasm Frequency Scale (PSFS)
| 40 weeks | 14 October 2024 | 23 July 2024 | 1 | |
| NCT06596369 | Transcutaneous Spinal Cord Stimulation for Upper Extremity Function | University of Alberta | | - Age 18 - 75 yrs
- Level C3-C8
AIS - ≥ 1 years
- NOT have active or inactive implants including cardiac pacemakers, implantable defibrillators, ocular implants, deep brain stimulators, vagus nerve stimulator, and implanted medication pumps
- NOT have conductive, ferromagnetic or other magnetic-sensitive metals implanted in their head
| Recruiting | 30 | PHASE2, PHASE3 | Technology | Arm/hand function | - Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
- Surface Electromyography (sEMG)
| 8 months | 15 June 2024 | 19 September 2024 | 2 | |
| NCT06520020 | Evaluating Safety and Feasibility of Transcutaneous Spinal Cord Stimulation Following Traumatic and Non-Traumatic Spinal Cord Injury: A Pilot Study | University of Kentucky | | - Age 18 - 80 yrs
- Level C2-T12
AIS A, B, C, D- 2 weeks - 24 months
- NOT have a cardiac pacemaker
- NOT have brain implant, skull prosthesis, plate and screws limiting transcranial stimulation
| Recruiting | 30 | NA | Technology | General health | - 10 Meter Walking Test (10 MWT)
- Adverse Events (AEs)
- American Spinal Injury Association Impairment Scale (AIS): International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
- Blood Pressure and Heart Rate Regulation
- Feasibility
- Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
- Spinal Cord Independence Measure (SCIM)
- World Health Organization Quality of Life- BREF (WHOQOL-BREF)
| 1 year | 23 October 2024 | 25 July 2024 | 1 | |
