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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
NCT06793683Early BOTOX After Spinal Cord InjuryUniversity of Washington
  • Age 18 - 65 yrs
  • Level C1-T6
  • AIS A, B
  • ≤ 20 weeks
By invitation10EARLY_PHASE1DrugBladder health/function
  • Adverse Events (AEs)
  • Feasibility
1 year27 July 202427 January 20251
NCT07343583Effects of Sacral and Tibial Stimulation on Bladder Function in Subacute Suprasacral Spinal Cord InjuryAnkara City Hospital Bilkent
  • Age 18 - 65 yrs
  • Level C1-T11
  • AIS
  • ≤ 6 months
  • NOT have a cardiac pacemaker
Recruiting45NATechnologyBladder health/function
  • Neurogenic Bladder Symptom Score
  • Neurogenic Bowel Dysfunction Score (NBD or NBDS)
  • Spinal Cord Independence Measure (SCIM)
  • Urodynamic examination
2 months05 August 202515 January 20261
NCT07359677High-frequency Alternating Current Stimulation for Neurophatic Pain in Spinal Cord InjuryUniversity of Castilla-La Mancha
  • Age ≥ 18 yrs
  • Level T1-S5
  • AIS A, B, C, D
  • ≥ 3 months
  • NOT have a cardiac pacemaker or any other implanted electrical device
Ended30NATechnologyPain
  • Adverse Events (AEs)
  • Ashworth and Modified Ashworth Scale (MAS)
  • Neuropathoc Pain Symptom Inventory (NPSI)
  • Pain Visual Analog Scale (VAS)
  • Penn Spasm Frequency Scale (PSFS)
15 days30 January 202622 January 20261
NCT07293780Effect of TMS on Neuropathic Pain for Patients With SciAnkara Etlik City Hospital
  • Age 18 - 65 yrs
  • Level C1-S5
  • AIS
  • ≥ 12 months
  • NOT have metallic implants in the scalp, cochlear implants, pacemaler or spinal cord stimulator
  • Have central, neuropathic pain.
Recruiting39NATechnologyPain
  • Beck Depression Inventory (BDI)
  • Pain Visual Analog Scale (VAS)
12 weeks15 December 202519 December 20252
NCT07357428Connect-One: Early Feasibility Study of Connexus® Brain-Computer Interface (BCI)Paradromics
  • Age 22 - 75 yrs
  • Level C1-T1
  • AIS
  • All
  • NOT have another implanted device, like a pacemaker, deep brain stimulator, or implantable pulse generator
  • Have impaired speech (dysarthria or anarthria)
Recruiting2NATechnologyGeneral health
  • Adverse Events (AEs)
6 years31 March 202622 January 20263
NCT07225582Development of Optimal Sensory Feedback Strategies to Maximize Function After TetraplegiaCase Western Reserve University
  • Age 22 - 65 yrs
  • Level C1-C8
  • AIS
  • ≥ 12 months
  • have already been enrolled in the in the "Reconnecting the Hand and Arm to the Brain (ReHAB)" Study (NCT03898804: https://www.scitrialsfinder.net/trials/NCT03898804)
Recruiting3NATechnologyArm/hand function2 years13 January 202606 November 20251