Neural Stem Cells Therapy for Cerebral Palsy
Primary Purpose
Cerebral Palsy
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
neural stem cells therapy group
the control group
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy
Eligibility Criteria
Inclusion Criteria:
- Neonates with ischemic/hypoxic cerebral palsy (mainly including neonate with asphyxia and premature infants);
- Clinical manifestation of spastic tetraplegia;
- With moderate to severe cerebral palsy, The Gross Motor Function; Classification System (GMFCS) levels IV-V;
- Age 1-5 years, of either sex;
- Provision of signed informed consent by one of his/her parents or legal guardians prior to commencement of this study;
Exclusion Criteria:
- Systemic diseases that possibly influence treatment or patient's compliance;
- Potentially life-threatening diseases involving various organ systems;
- Brain deformity;
- Abnormal behaviors or mood disorder;
- Allergies from blood products;
- Suffering from infectious disease;
- Subjected to craniocerebral operations prior to screening.
Sites / Locations
- The First Affiliated Hospital of Dalian Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
neural stem cells therapy group
the control group
Arm Description
The patients will be assigned to neural stem cells therapy group for cerebral palsy.
The patients will be assigned to the control group for cerebral palsy.
Outcomes
Primary Outcome Measures
GMFM-88 score
To evaluate change in gross motor function in children with cerebral palsy.
Secondary Outcome Measures
Fine Motor Function Measure (FMFM) score
To evaluate change in fine motor function in children with cerebral palsy.
Modified Ashworth Scale score
To measure resistance during passive soft-tissue stretching and is used as a simple measure of spasticity.
Full Information
NCT ID
NCT03005249
First Posted
December 26, 2016
Last Updated
August 27, 2018
Sponsor
The First Affiliated Hospital of Dalian Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03005249
Brief Title
Neural Stem Cells Therapy for Cerebral Palsy
Official Title
Neural Stem Cells Therapy for Cerebral Palsy: a Prospective, Randomized, Parallel-controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (undefined)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital of Dalian Medical University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To evaluate the safety and efficacy of neural stem cells (NSCs) therapy for cerebral palsy.
Detailed Description
Cerebral palsy is the most severe lifelong disability disease in childhood. In China, an epidemiological investigation of cerebral palsy in 2004 has reported that 2.74‰ (about 6.50-9.75 million) of children suffered from cerebral palsy. The costs of medical expenses, living allowance and nursing care can go up to RMB 20000-50000 yuan per year for each child with cerebral palsy and thus China will expend RMB 120-300 billion yuan per year for children with cerebral palsy. With full liberalization of two-child policy, there is an increasing number of second babies born to women who are 35 years or older. Thus, the incidence of cerebral palsy tends to increase. There is currently no cure for cerebral palsy, resulting in a heavy burden for families and on society. Recent clinical trials performed in countries outside China have demonstrated that stem cell therapy is likely the most effective method to treat cerebral palsy. Fifteen trials regarding stem cell therapy for cerebral palsy have been registered with ClinicalTrials.gov. In China, there have been no standardized registered trials regarding stem cell therapy for cerebral palsy, which greatly restricts its clinical application. In October 2016, the National Health and Family Planning Commission and the Food and Drug Administration of China jointly announced the premier stem cell clinical research institutions, making performing standardized trials regarding stem cell therapy for cerebral palsy in China possible.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
neural stem cells therapy group
Arm Type
Experimental
Arm Description
The patients will be assigned to neural stem cells therapy group for cerebral palsy.
Arm Title
the control group
Arm Type
Experimental
Arm Description
The patients will be assigned to the control group for cerebral palsy.
Intervention Type
Procedure
Intervention Name(s)
neural stem cells therapy group
Intervention Description
The patients will be assigned to neural stem cells therapy group for cerebral palsy.
Intervention Type
Other
Intervention Name(s)
the control group
Intervention Description
The patients will be assigned to the control group for cerebral palsy.
Primary Outcome Measure Information:
Title
GMFM-88 score
Description
To evaluate change in gross motor function in children with cerebral palsy.
Time Frame
changes of month 1, month 3, month 6, month 9 and month 12 after therapy
Secondary Outcome Measure Information:
Title
Fine Motor Function Measure (FMFM) score
Description
To evaluate change in fine motor function in children with cerebral palsy.
Time Frame
changes of month 1, month 3, month 6, month 9 and month 12 after therapy
Title
Modified Ashworth Scale score
Description
To measure resistance during passive soft-tissue stretching and is used as a simple measure of spasticity.
Time Frame
changes of month 1, month 3, month 6, month 9 and month 12 after therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Neonates with ischemic/hypoxic cerebral palsy (mainly including neonate with asphyxia and premature infants);
Clinical manifestation of spastic tetraplegia;
With moderate to severe cerebral palsy, The Gross Motor Function; Classification System (GMFCS) levels IV-V;
Age 1-5 years, of either sex;
Provision of signed informed consent by one of his/her parents or legal guardians prior to commencement of this study;
Exclusion Criteria:
Systemic diseases that possibly influence treatment or patient's compliance;
Potentially life-threatening diseases involving various organ systems;
Brain deformity;
Abnormal behaviors or mood disorder;
Allergies from blood products;
Suffering from infectious disease;
Subjected to craniocerebral operations prior to screening.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jing Liu, Ph.D
Phone
86041184394568
Email
liujing.dlrmc@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jing Liu, Ph.D
Organizational Affiliation
The First Affiliated Hospital of Dalian Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The First Affiliated Hospital of Dalian Medical University
City
Dalian
State/Province
Liaoning
ZIP/Postal Code
116011
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jing Liu, Ph.D
Phone
86041184394568
Email
liujing.dlrmc@hotmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Neural Stem Cells Therapy for Cerebral Palsy
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