All trials - page: 24

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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
NCT06907381Blood Flow-restricted Resistance Exercise to Promote Muscle Strength and Use in Adults With Incomplete Spinal Cord InjuryQuality Living, Inc.
  • Age 19 - 70 yrs
  • Level C1-C8
  • AIS
  • All
By invitation10Arm/hand function
  • Functional Independence Measure (FIM)
6 months01 April 202502 April 20251
NCT06908850The Aim of This Research is to Better Understand How Complete Spinal Cord Injury May Change Erogenous Zones in Adult MalesFondation Garches
  • Age ≥ 18 yrs
  • Level C1-S5
  • AIS
  • All
By invitation15Sexual health0 days17 March 202503 April 20251
NCT06939634Evaluation of Usability and Safety of the System Atalante in Patients With High Paraplegia and TetraplegiaWandercraft
  • Age ≥ 18 yrs
  • Level C1-T4
  • AIS
  • All
Ended35Standing/walking/mobility
  • 10 Meter Walking Test (10 MWT)
  • 2 Minute Walk Test
  • Adverse Events (AEs)
  • Berg Balance Scale (BBS)
  • Spinal Cord Independence Measure (SCIM)
  • Timed Up and Go Test (TUG)
  • Walking Index for Spinal Cord Injury (WISCI) and WISCI II
101 weeks01 June 202423 April 20254
NCT06943040Validity and Reliability of 6-minute Pegboard and Ring TestIstinye University
  • Age 18 - 70 yrs
  • Level T1-L5
  • AIS
  • ≥ 1 years
  • be a full-time wheelchair user
Recruiting soon34Arm/hand function
  • Barthel Index (BI)
  • Modified Functional Reach Test (mFRT)
1 week28 April 202524 April 20250
NCT06700278Auricular Acupressure and Limb Massage for Neuropathic Pain in Spinal Cord InjuryNational Taiwan University Hospital
  • Age ≥ 18 yrs
  • Level C1-S5
  • AIS B, C, D
  • ≤ 12 months
  • NOT have previously undergone nerve block surgery
Recruiting soon90NAPsychosocial/otherPain
  • Barthel Index (BI)
  • World Health Organization Quality of Life- BREF (WHOQOL-BREF)
3 weeks01 April 202521 November 20240
NCT06493071Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) for Inflammation and Depression Following SCILondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • Age ≥ 18 yrs
  • Level C1-S5
  • AIS
  • All
  • NOT have a pacemaker or other implanted electrical device (e.g. cochlear implant, implanted vagus nerve stimulator, cardiac pacemaker)
  • have mild to moderate measures for depression
Recruiting44NATechnologyGeneral health
  • Adverse Events (AEs)
  • Patient Health Questionnaire-9 (PHQ-9)
30 days27 January 202509 July 20241