Cerebral Palsy, Spastic Clinical Trial
Official title:
Evaluation of the Efficacy of Allogeneic Umbilical Cord Derived Hematopoietic Stem Cells and Mesenchymal Stromal Cells in Patients With Spastic Cerebral Palsy on Developmental Function , A Clinical Trial phase2
Cerebral palsy(CP) consisted of a group of developmental disability in the field of motor function and is one of the major problems of pediatric neurology and at the present time there is no standard curative medical or surgical treatment for it .Stem cell therapy is one of a new and hopeful therapeutic methods of therapy for CP .This double blind study designed for the evaluation of safety and therapeutic effects of intrathecal hematopoietic and mesenchymal stem cells derived from allogenic umbilical cord in change and probable improvement of developmental functions of spastic CP participants between 4-14 years old and comparing with control group of CP participants without cell therapy . 108 cases recruited and randomly divided to 3 groups of 36 cases : hematopoietic stem cells derived from allogenic umbilical cord , Mesenchymal cells derived from allogenic umbilical cord and control group without injection and appearance simulating lumbar puncture without awareness of the patients and evaluators . Developmental functions and spasticity evaluated before intervention and will be done 1 , 3 , 6 and 12 months after injection . During this period neuro rehabilitation will be continued . Brain neuroimaging were done at the recruitment time and will be repeated after 12 months .
CP is characterized by aberrant control of movement or posture of a patient , appearing early
in life , and not the result of a recognized progressive or degenerative brain disease . CP
is an umbrella term and represents a group of conditions (not a single disorder) , has a
broad range of expression with a static condition originally within the developing central
nervous system . CP Is a disturbance of movement and or posture . At the present time there
is no standard medical or surgical treatment for it .Stem cell therapy is a new and promising
treatment .
150 cases of diparetic and quadiparetic spastic CP between 4-14 years old selected among the
patients referred to the pediatric neurology outpatient department of Children's Medical
Center Hospital (CMC) affiliated to Tehran University of Medical Sciences and had our
inclusion criteria. HLA analysis were done for these patients and 36 cases of class 6 matched
cases enrolled to the hematopoietic stem cells derived from allogenic umbilical cord (MNC)
because of necessity of Human Leukocyte Antigen (HLA) matching in this type of cells and 72
cases among the remaining patients randomly divided to Mesenchymal stem cells derived from
allogenic umbilical cord (MSC) and control group . Therefore 108 cases enrolled in 3 divided
group of 36 patients .
Patients admitted to CMC hospital and intrathecal injection were done with sedation . Only
one injection of stem cell was done for each patient . In the control group after insertion
of the needle into the skin with an appearance of lumbar puncture simulation , no injection
were done without the awareness of the patients or their parents. All of the patients
admitted for one day and discharged the next day . As we wrote in the consent form for
ethical consideration we are committed to perform stem cell injection for control
participants free of charge after 12 months of the follow up . All of the participants will
be referred for neurorehabilitation with a identical protocol .Both parents and clinical
evaluators are not aware of the 3 divided groups and our study is double blind .Outcome
measures will be evaluated 1, 3, 6. and 12 months after intervention .
Standard brain Magnetic Resonance Imaging (MRI) with Magnetic Resonance Spectroscopy (MRS)
and Diffusion Tensor Imaging (DTI) were done before injection as baseline and will be
repeated after 12 months of clinical follow up . This study designed for the evaluation of
therapeutic effects of intrathecal MNC and MSC derived from allogenic umbilical cord in
change and probable improvement of developmental functions of spastic CP patients between
4-14 years old in comparison with control group .Different scoring systems such as Gross
Motor Functional Classification System (GMFCS) , Gross Motor Function Measure Score (GMFM66)
, Manual Ability Classification System (MACS) , Pediatric Evaluation of Disability Inventory
(PEDI) , CP QOL , Life Habits Questionnaire and Modified Ashworth scale for spasticity were
done at baseline and then will be repeated in follow ups until 12 months of final evaluation
.
Acute side effects and probable long term side effects will be reported and noted on our
preformed questioners .
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