37
Participants
Start Date
February 29, 2012
Primary Completion Date
July 31, 2012
Study Completion Date
July 31, 2012
Umbilical Cord Blood Infusion
The subjects will be undertaken allogeneic umbilical cord blood infusion intravenously or intraarterially under non-myeloablative immunosuppression.
Placebo Umbilical Cord Blood
Placebo Umbilical Cord Blood that resembles cord blood in appearance was designed.
Active Rehabilitation
All subjects should participate in active rehabilitation. They will receive two physical and occupational therapy sessions per day. Post discharge, each participant should continue to receive rehabilitation therapy at least 3 days per week until the study completion.
CHA Bundang Medical Center, CHA University, Seongnam-si
MinYoung Kim, M.D.
OTHER