Autologous Adipose Derived MSCs Transplantation in Patient With Spinal Cord Injury. (MSC)
Primary Purpose
Spinal Cord Injury
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Autologous Adipose Derived Mesenchymal Stem Cells
Sponsored by
About this trial
This is an interventional treatment trial for Spinal Cord Injury
Eligibility Criteria
Inclusion Criteria:
- Subjects who understand and sign the consent form for this study.
- Age :19-60, males
- Clinical diagnosis of spinal cord injury(American Spinal Injury Association[ASIA] Impairment Scale[AIS] grade A or B or C)
- Duration of injury : > 2 months
Exclusion Criteria:
- Subjects who must put on a respirator
- Subjects who had malignant tumor within 5 years
- Subjects with a infectious disease include HIV and hepatitis
- Subjects who injured brain or spinal cord before spinal cord injury
- Subjects who has high body temperature more than 38℃ or acute disorder
- Subjects with anemia or thrombocytopenia
- Subjects with angina pectoris, myocardial infarction, cardiomyopathy, occlusive disease, chronic renal failure, glomerular disease and chronic obstructive pulmonary disease
- Subjects with congenital or acquired immunodeficiency disorders
- Subjects with muscular dystrophy or articular rigidity
- Patients with clouded consciousness or speech disorder
- treat with cytotoxic medications(immunosuppressive drug, corticosteroid and cytotoxic drug) during clinical trials
- participating another clinical trials within 3 months
- other serious disease or disorder that could seriously affect ability to participate in the study
Sites / Locations
Outcomes
Primary Outcome Measures
safety evaluation
Safety evaluate through physical examination, vital sign and laboratory test after "RNL-Astrostem" injected
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01274975
Brief Title
Autologous Adipose Derived MSCs Transplantation in Patient With Spinal Cord Injury.
Acronym
MSC
Official Title
Safety of Autologous Adipose Derived Mesenchymal Stem Cells in Patients With Spinal Cord Injury
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
July 2009 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
February 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
R-Bio
4. Oversight
5. Study Description
Brief Summary
This study is designed to assess the safety of intravenous autologous adipose derived mesenchymal stem cells transplant in spinal cord injury patients.
Detailed Description
Adipose derived mesenchymal stem cells (AdMSCs) represent an attractive and ethical cell source for stem cell therapy.
With the recent demonstration of MSC homing properties, intravenous aplications of MSCs to cell-damaged diseases have increased.
In a human clinical trial, eight male patients who had suffered a spinal cord injury were intravenously administered autologous hAdMSCs (4×10e8 cells) one time.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
Autologous Adipose Derived Mesenchymal Stem Cells
Other Intervention Name(s)
Astrostem®
Intervention Description
Intravenous infusion of Autologous Adipose Derived Mesenchymal Stem Cells. Dose : 4 x 10e8 cells
Primary Outcome Measure Information:
Title
safety evaluation
Description
Safety evaluate through physical examination, vital sign and laboratory test after "RNL-Astrostem" injected
Time Frame
12weeks
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects who understand and sign the consent form for this study.
Age :19-60, males
Clinical diagnosis of spinal cord injury(American Spinal Injury Association[ASIA] Impairment Scale[AIS] grade A or B or C)
Duration of injury : > 2 months
Exclusion Criteria:
Subjects who must put on a respirator
Subjects who had malignant tumor within 5 years
Subjects with a infectious disease include HIV and hepatitis
Subjects who injured brain or spinal cord before spinal cord injury
Subjects who has high body temperature more than 38℃ or acute disorder
Subjects with anemia or thrombocytopenia
Subjects with angina pectoris, myocardial infarction, cardiomyopathy, occlusive disease, chronic renal failure, glomerular disease and chronic obstructive pulmonary disease
Subjects with congenital or acquired immunodeficiency disorders
Subjects with muscular dystrophy or articular rigidity
Patients with clouded consciousness or speech disorder
treat with cytotoxic medications(immunosuppressive drug, corticosteroid and cytotoxic drug) during clinical trials
participating another clinical trials within 3 months
other serious disease or disorder that could seriously affect ability to participate in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
SangHan Kim, MD
Organizational Affiliation
Anyang Sam Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
21303266
Citation
Ra JC, Shin IS, Kim SH, Kang SK, Kang BC, Lee HY, Kim YJ, Jo JY, Yoon EJ, Choi HJ, Kwon E. Safety of intravenous infusion of human adipose tissue-derived mesenchymal stem cells in animals and humans. Stem Cells Dev. 2011 Aug;20(8):1297-308. doi: 10.1089/scd.2010.0466. Epub 2011 Mar 17.
Results Reference
result
Learn more about this trial
Autologous Adipose Derived MSCs Transplantation in Patient With Spinal Cord Injury.
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