This study will evaluate the effect of single transplantation of HuCNS-SC cells into the
thoracic spinal cord of patients with sub-acute spinal cord injury.
Biological: HuCNS-SC cells
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Locations near you
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Full eligibility criteria for NCT01321333
Ages eligible for Study
18 Years to 60 Years
Genders eligible for Study
Accepts Healthy Volunteers
T2-T11 thoracic spinal cord injury based on American Spinal Injury Association (ASIA) level determination by the principal investigator (PI)
T2-T11 thoracic spinal cord injury as assessed by magnetic resonance imaging (MRI) and/or computerized tomography (CT)
ASIA Impairment Scale (AIS) Grade A, B, or C
Minimum of six weeks post injury for the initiation of screening
Must have evidence of preserved conus function
Must be at stable stage of medical recovery after injury
History of traumatic brain injury without recovery
Penetrating spinal cord injury
Evidence of spinal instability or persistent spinal stenosis and/or compression related to initial trauma
Previous organ, tissue or bone marrow transplantation
Previous participation in any gene transfer or cell transplant trial
Current or prior malignancy
All locations for NCT01321333
Foothills Medical Center
Calgary, Alberta, Canada, T2N-2T9
Toronto Western Hospital
Toronto, Ontario, Canada
University Hospital Balgrist- Uniklinik Balgrist, Forschstrasse 340
Zurich, Switzerland, 8008
View full eligibility
Tris trial is registered with FDA with number: NCT01321333. The sponsor of the trial is StemCells, Inc. and it is looking for 12 volunteers for the current phase.
Official trial title: A Phase I/II Study of the Safety and Preliminary Efficacy of Intramedullary Spinal Cord Transplantation of Human Central Nervous System (CNS) Stem Cells (HuCNS-SC®) in Subjects With Thoracic (T2-T11) Spinal Cord Trauma
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