All trials - page: 41

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NCTID
Brief title
Sponsor
Design
Criteria
Status
Target enrollment
Study phase & design
Primary intervention type
Primary potential benefit
Outcome measure
Follow up
Start date
First posted
Location
NCT06740279Investigating 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 soon210Arm/hand function6 months07 January 202518 December 20240
NCT06511934Feasibility 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)
Recruiting2NATechnologyGeneral health
  • Adverse Events (AEs)
  • Feasibility
1 year22 July 202422 July 20241
NCT06515223Improving Pelvic Rehabilitation Using Epidural Stimulation After Spinal Cord InjuryUniversity 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
Recruiting20NATechnologyBladder health/function
  • American Spinal Injury Association Impairment Scale (AIS)
  • Bowel and bladder control
  • European Quality of Life Five Dimension Five Level Scale (EQ-5D-5L)
  • International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
  • Neurogenic Bladder Symptom Score
  • Neurogenic Bowel Dysfunction Score (NBD or NBDS)
  • Penn Spasm Frequency Scale (PSFS)
40 weeks14 October 202423 July 20241
NCT06596369Transcutaneous Spinal Cord Stimulation for Upper Extremity FunctionUniversity 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
Recruiting30PHASE2, PHASE3TechnologyArm/hand function
  • Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
  • Surface Electromyography (sEMG)
8 months15 June 202419 September 20242
NCT06520020Evaluating Safety and Feasibility of Transcutaneous Spinal Cord Stimulation Following Traumatic and Non-Traumatic Spinal Cord Injury: A Pilot StudyUniversity 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
Recruiting30NATechnologyGeneral health
  • 10 Meter Walking Test (10 MWT)
  • Adverse Events (AEs)
  • American Spinal Injury Association Impairment Scale (AIS)
  • Blood Pressure and Heart Rate Regulation
  • Feasibility
  • Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
  • International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
  • Spinal Cord Independence Measure (SCIM)
  • World Health Organization Quality of Life- BREF (WHOQOL-BREF)
1 year23 October 202425 July 20241
NCT06583538An Online Rehabilitation Programme for People with SCIGlasgow Caledonian University
  • Age ≥ 18 yrs
  • Level C1-S5
  • AIS
  • ≤ 1 years
  • be an inpatient at the Queen Elizabeth National Spinal Injuries Unit
Ended15NARehabilitationGeneral health
  • Feasibility
  • Physical Activity Scale for Individuals with Physical Disabilities (PASIPD)
  • Spinal Cord Independence Measure (SCIM)
  • Walking Index for Spinal Cord Injury (WISCI) and WISCI II
  • World Health Organization Quality of Life- BREF (WHOQOL-BREF)
12 weeks22 November 202304 September 20241