All trials - page: 252

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NCTID
Brief title
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Design
Criteria
Status
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Study phase & design
Primary intervention type
Primary potential benefit
Outcome measure
Follow up
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Location
NCT02688049NeuroRegen Scaffold™ Combined With Stem Cells for Chronic Spinal Cord Injury RepairChinese Academy of Sciences
  • Age 18 - 65 yrs
  • Level C5-T12
  • AIS A
  • ≥ 0 hours
  • have a chronic spinal cord injury
  • have a neurological level of injury between C5 and Th12
  • have the following ASIA impairment scale (AIS) classifications:
  • AIS A: complete; no feeling or movement below the injury with no evidence of further improvement.
  • be between 18 and 65 years of age
  • be able and willing to attend scheduled follow-up visits over 24 months at the study center (Tianjin, China).
30PHASE1, PHASE2Biological/cell basedArm/hand function01 January 201623 February 20161
NCT02673320Prospective Study for Delay in Surgical Treatment of Traumatic Cervical Central Cord Injury in Canal StenosisNantes University HospitalParallel Assignment
  • Age ≥ 18 yrs
  • Level C1-T1
  • AIS A, B, C, D
  • ≤ 15 days
  • have an acute spinal cord injury capable of undergoing surgical decompression within 48 hours at the time of randomization.
  • have a neurological level of injury between C2-T1
  • have one of the following ASIA impairment scale (AIS):
  • AIS A: complete; no feeling or movement below the injury
  • AIS B: incomplete; have some feeling, but no movement, below the injury
  • AIS C: incomplete; at least some feeling and mostly weak movement below the injury
  • AIS D: incomplete; at least some feeling and, some weak but mostly stronger movement below the injury
  • be at least 18 years of age
  • be able to undergo an MRI
Recruiting72Not ApplicableSurgeryStanding/walking/mobility01 July 201603 February 20168
NCT02611375Conditioning Neural Circuits to Improve Upper Extremity FunctionShepherd Center, Atlanta GA
  • Age 18 - 65 yrs
  • Level C1-C8
  • AIS A, B, C, D
  • ≤ 65 years
  • must have some trouble moving at least one of your arms/hands.
  • must be able to pick up an object with at least one hand without any type of help.
  • be able to lift one arm up to chest level.
  • NOT have other implanted device, e.g. pacemaker
  • NOT have history of epilepsy or severe headaches
Ended80NATechnologyArm/hand function09 February 201720 November 20151
NCT02574585Autologous Mesenchymal Stem Cells Transplantation in Thoracolumbar Chronic and Complete Spinal Cord Injury Spinal Cord InjuryHospital Sao Rafael
  • Age 18 - 65 yrs
  • Level T1-L2
  • AIS A
  • 12 months - 65 years
  • NOT have diabetes mellitus type 1 or 2
  • NOT have SCI due to sharp object or firearm
  • NOT have other metallic implant that would affect MRI
40PHASE2Biological/cell basedStanding/walking/mobility01 December 201914 October 20150
NCT02574572Autologous Mesenchymal Stem Cells Transplantation in Cervical Chronic and Complete Spinal Cord InjuryHospital Sao Rafael
  • Age 18 - 65 yrs
  • Level C5-C7
  • AIS A
  • 12 months - 65 years
  • have a spinal cord injury for at least 12 months
  • have a neurological level of injury between C5 and C7
  • have the following ASIA impairment scale (AIS) grade:
  • AIS A: complete; no feeling or movement below the injury
  • be between 18 and 65 years of age
  • NOT have penetrating injury, e.g. gunshot or knife wound
  • NOT have other device implanted that would affect MRI, e.g. pacemaker
10PHASE1Biological/cell basedGeneral health06 September 201714 October 20151
NCT02566850Investigational Study of the Ekso for High-Dosage Use by Individuals With SCI in a Non-Clinical EnvironmentEkso Bionics
  • Age 18 - 65 yrs
  • Level C1-S5
  • AIS A, B, C, D
  • 1 months - 65 years
  • have a body height between 152 and 193cm (5’-6’33 feet)
  • have a body weight of less than 100kg (<200 lbs)
  • have a prior experience or be willing to train on the Ekso device with a minimum of 20 hours and no more than 50 hours of device use and require no greater than minimal assist (support of up to 25% body weight) for safe and consistent walking. Participants with more than 50 hours of device experience must agree to a 1 month period of non-use prior to acquisition of baseline measures
Ended4NARehabilitationGeneral health01 January 201402 October 20151