Treating Center of Spinal Cord Injury, Chinese PLA Chengdu Army Kunming General Hospital
Kunming, Yunnan, 650032, China
NCT Number: NCT01471613
The trial is to investigate the safety and efficacy of oral lithium, intraspinal umbilical cord blood mononuclear cell transplant, and the combination in the treatment of acute and subacute spinal cord injury
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Phase 1 / Phase 2
Kunming, Yunnan, 650032, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Conventional treatment includes surgeries such as laminectomy, spinal decompression etc. and the medicine generally adapted to treat spinal cord injury
250mg/tablet, administrated orally for 6 weeks.
Cord blood mononuclear cell, 6.4 million viable cells, are transplanted into spinal cord at upper and lower edges of the injured site
Placebo tablet, orally administration of placebo for 6 weeks
Time frame: Week 0, 1, 2, 6, 14, 24 and 48
Time frame: Week 2, 6, 14, 24, 48
Walking Index of Spinal Cord Injury (WISCI)
Time frame: Week 2, 6, 14, 24, 48
Spinal Cord Injury Measure (SCIM) Score
Time frame: Week 2, 6, 14, 24, 48
Kunming locomotor scales
Time frame: Week 2, 6, 14, 24, 48
Modified Ashworth Scale
Time frame: Week 2, 6, 14, 24, 48
Numerical rating scales
Looking for future studies?
Notify MeChina Spinal Cord Injury Network
Network
Safety and Effect of Lithium, Umbilical Cord Blood Cells and the Combination in the Treatment of Acute and Sub-acute Spinal Cord Injury : a Randomized, Double-Blinded Placebo-Controlled Clinical Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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