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Transplantation of Umbilical Cord-derived Mesenchymal Stem Cells Via Different Routes

Primary Purpose

Cerebral Palsy

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Control group
UC-MSCs
Sponsored by
The First Affiliated Hospital of Dalian Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Palsy focused on measuring umbilical cord-derived mesenchymal stem cells, cerebral palsy

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with hypoxic/ischemic cerebral palsy, primarily including birth asphyxia and premature children
  • Patients with spastic quadriplegia
  • Patients with moderate to severe cerebral palsy, GMFM scores of 2-3
  • Age at 2-18 years
  • Provision of signed informed consent by legal representatives of the child prior to start of the study

Exclusion Criteria:

  • Those with systemic diseases that likely interfere with the treatment or child's compliance
  • Those complicated by life-threatening diseases of any organ
  • Those with brain deformity
  • Those with uncontrolled epilepsy
  • Those with abnormal behavior or mood disorders
  • Those with allergies especially those who are allergic to blood products
  • Those are infected with infectious diseases
  • Those who had underwent a craniocerebral surgery in other clinical trials

Sites / Locations

  • The First Affiliated Hospital of Dalian Medical University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Experimental

Experimental

Experimental

Arm Label

Control group

Intravenous UC-MSCs group

Intrathecal UC-MSCs group

Intranasal UC-MSCs group

Arm Description

Routine rehabilitation treatments

Injection of UC-MSCs via the peripheral vein.

Injection of UC-MSCs via the intrathecal route.

Injection of UC-MSCs via the nasal route.

Outcomes

Primary Outcome Measures

The Gross Motor Function Measure (GMFM)-88 item score
a 4-point scale that is divided into five categories including lying and rolling, sitting, crawling and kneeling, standing, walking, running, and jumping. A score of 0 indicates that the child does not initiate the task; 1 indicates that the child initiates the task (completes < 10% of the activity); 2 indicates that the child partially completes the task (completes from 10 to 99% of the activity); 3 indicates that the child completes the task (100%). The sum of score of the five categories is used as the evaluation outcome.It is used to evaluate gross motor function.

Secondary Outcome Measures

Fine Motor Function Measure scale (FMFM) score
To evaluate fine motor function.The scale is divided into 45 items covering visual tracing (7 items), upper extremity range of motion (8 items), grab ability (8 items), operational ability (10 items), and hand-eye coordination (12 items). The FMFM is a 4-point scale with the score range of 0-3. The original total score is 135. The summed score for evaluating fine motor function measure is 0-100.
The Modified Ashworth scale (MAS) score
To evaluate muscle tone. The MAS score is divided into six grades: 0, 1, 1+, 2, 3 and 4. Passive full ranges of motion exercises are performed by moving the knee and ankle until the patient feel a slight resistance from hamstrings and plantar flexor muscles (soleus muscle and gastrocnemius muscle). The average score is calculated across three repeated measurements.
Gesell Development Schedule score
To evaluate neurobehavioral development.
Incidence of adverse reactions
Liver and kidney dysfunction, fever, infection, vomiting.

Full Information

First Posted
January 22, 2018
Last Updated
January 26, 2018
Sponsor
The First Affiliated Hospital of Dalian Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03414697
Brief Title
Transplantation of Umbilical Cord-derived Mesenchymal Stem Cells Via Different Routes
Official Title
Transplantation of Umbilical Cord-derived Mesenchymal Stem Cells Via Different Routes for the Treatment of Cerebral Palsy in Children
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
April 2018 (Anticipated)
Primary Completion Date
September 2020 (Anticipated)
Study Completion Date
December 2020 (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

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To preliminarily evaluate the efficacy and safety of umbilical cord-derived mesenchymal stem cells (UC-MSCs), and compare the efficacy of UC-MSCs administered through the intravenous, intrathecal, and intranasal routes, in the treatment of cerebral palsy in children.
Detailed Description
Cerebral palsy refers to a neurological disorder caused by a non-progressive brain injury or malformation that occurs in early childhood. It can result in central motor deficits, developmental retardation, abnormal posture, abnormal muscular strength, abnormal muscle tone and/or dysreflexia. It has a high disability rate. There is currently no effective treatment for cerebral palsy. Conventional treatments for cerebral palsy are often tiresome and expensive and have a slow onset of action. Stem cells have been recently used in the treatment of cerebral palsy. This provides a novel method for the treatment of cerebral palsy. According to the existing clinical studies, neural stem cells, bone marrow-derived mesenchymal stem cells, and umbilical cord-derived mesenchymal stem cells (UC-MSCs) are mainly used as the seed cells for the treatment of cerebral palsy. UC-MSCs are the most promising seed cells for the treatment of cerebral palsy because of the advantages including rich sources, ease of harvesting, short doubling time, low immunogenicity, long-time survival post-transplantation, and no ethical issues. UC-MSCs have been widely used to treat Parkinson's disease, rheumatoid arthritis, traumatic brain injury, aplastic anemia, and decompensated liver disease. However,only two studies, and performed only in China, are reported on the treatment of cerebral palsy with UC-MSCs. One from the Hospital 463 of PLA reported 51 patients with cerebral palsy whose symptoms had not been obviously improved after 1 year of rehabilitative treatment. These patients received intrathecal injection of UC-MSCs for three times, once a week, followed by one injection of UC-MSCs via the peripheral vein in the fourth week. Four UC-MSCs injections, once per week, were considered as one course of treatment. Activities of daily living scale score was compared between before and after treatment to evaluate efficacy. Another study is a case report from China. In this report, a combined intravenous and intrathecal injection of UC-MSCs was used to treat cerebral palsy in a 5-year-old child. 28-month follow-up results revealed that the child's gross motor function, immune function, muscle strength, and language ability improved and adverse reactions were not obvious.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
umbilical cord-derived mesenchymal stem cells, cerebral palsy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Other
Arm Description
Routine rehabilitation treatments
Arm Title
Intravenous UC-MSCs group
Arm Type
Experimental
Arm Description
Injection of UC-MSCs via the peripheral vein.
Arm Title
Intrathecal UC-MSCs group
Arm Type
Experimental
Arm Description
Injection of UC-MSCs via the intrathecal route.
Arm Title
Intranasal UC-MSCs group
Arm Type
Experimental
Arm Description
Injection of UC-MSCs via the nasal route.
Intervention Type
Other
Intervention Name(s)
Control group
Intervention Description
The control group received routine rehabilitation treatments including acupuncture, massage, Bobath therapy, and Vojat therapy.
Intervention Type
Procedure
Intervention Name(s)
UC-MSCs
Intervention Description
Injection of umbilical cord-derived mesenchymal stem cells (UC-MSCs) (at least 1×10^7), once every 2 weeks, one course of treatment including two injections within 4 weeks, a total of two courses of treatment.
Primary Outcome Measure Information:
Title
The Gross Motor Function Measure (GMFM)-88 item score
Description
a 4-point scale that is divided into five categories including lying and rolling, sitting, crawling and kneeling, standing, walking, running, and jumping. A score of 0 indicates that the child does not initiate the task; 1 indicates that the child initiates the task (completes < 10% of the activity); 2 indicates that the child partially completes the task (completes from 10 to 99% of the activity); 3 indicates that the child completes the task (100%). The sum of score of the five categories is used as the evaluation outcome.It is used to evaluate gross motor function.
Time Frame
12 months after 2 courses of treatment with UC-MSCs.
Secondary Outcome Measure Information:
Title
Fine Motor Function Measure scale (FMFM) score
Description
To evaluate fine motor function.The scale is divided into 45 items covering visual tracing (7 items), upper extremity range of motion (8 items), grab ability (8 items), operational ability (10 items), and hand-eye coordination (12 items). The FMFM is a 4-point scale with the score range of 0-3. The original total score is 135. The summed score for evaluating fine motor function measure is 0-100.
Time Frame
1, 3, 6, 9 and 12 months after 2 courses of treatment with UC-MSCs.
Title
The Modified Ashworth scale (MAS) score
Description
To evaluate muscle tone. The MAS score is divided into six grades: 0, 1, 1+, 2, 3 and 4. Passive full ranges of motion exercises are performed by moving the knee and ankle until the patient feel a slight resistance from hamstrings and plantar flexor muscles (soleus muscle and gastrocnemius muscle). The average score is calculated across three repeated measurements.
Time Frame
1, 3, 6, 9 and 12 months after 2 courses of treatment with UC-MSCs.
Title
Gesell Development Schedule score
Description
To evaluate neurobehavioral development.
Time Frame
1, 3, 6, 9 and 12 months after 2 courses of treatment with UC-MSCs.
Title
Incidence of adverse reactions
Description
Liver and kidney dysfunction, fever, infection, vomiting.
Time Frame
1, 3, 6, 9 and 12 months after 2 courses of treatment with UC-MSCs.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with hypoxic/ischemic cerebral palsy, primarily including birth asphyxia and premature children Patients with spastic quadriplegia Patients with moderate to severe cerebral palsy, GMFM scores of 2-3 Age at 2-18 years Provision of signed informed consent by legal representatives of the child prior to start of the study Exclusion Criteria: Those with systemic diseases that likely interfere with the treatment or child's compliance Those complicated by life-threatening diseases of any organ Those with brain deformity Those with uncontrolled epilepsy Those with abnormal behavior or mood disorders Those with allergies especially those who are allergic to blood products Those are infected with infectious diseases Those who had underwent a craniocerebral surgery in other clinical trials
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
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jing Liu, Ph.D
Phone
86041184394568
Email
liujing.dlrmc@hotmail.com

12. IPD Sharing Statement

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Transplantation of Umbilical Cord-derived Mesenchymal Stem Cells Via Different Routes

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