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Autologous Mesenchymal Stem Cells Transplantation for Spinal Cord Injury- A Phase I Clinical Study

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Phase 1
Locations
Pakistan
Study Type
Interventional
Intervention
mesenchymal stem cells
Sponsored by
National Institute of Blood and Marrow Transplant (NIBMT), Pakistan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injury focused on measuring Spinal cord injury, mesenchymal stem cells, transplantation

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients suffering from sub-acute and chronic phase of spinal cord injury
  • Traumatic spinal cord injury at the thoracic level
  • American Spinal Injury Association (ASIA) impairment scale "A"
  • Confirmation by MRI of injury level
  • Time between injury and enrollment greater than 2 weeks
  • Ability to provide informed consent

Exclusion Criteria:

  • Axonic brain injury
  • Inability to provide consent
  • Open injuries
  • Active infectious diseases
  • Terminal patients
  • Neurodegenerative diseases
  • Evidence of meningitis
  • Cerebral palsy
  • Primary haematologic diseases
  • Coagulopathies
  • Pregnancy
  • Other medical complications that contra-indicate surgery, including major respiratory complications
  • Use of metal implants close to vascular structures (such as cardiac pacemaker or prosthesis) that contraindicate MRI.

Sites / Locations

  • Armed Forces Bone Marrow Transplant Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Autologous mesenchymal stem cells

Arm Description

use of mesenchymal stem cells as therapeutic intervention for spinal cord injury patients by autologous transplantation

Outcomes

Primary Outcome Measures

Number of adverse events
Number of adverse events occurring in given time frame shall be reported to evaluate overall safety of the procedure

Secondary Outcome Measures

Sensory and motor strength
Improvement in sensitivity and motor strength will be measured through change in American Spinal Injury Association (ASIA) score from baseline
Functional Independence
Functional Independence will be measured by FIM scoring
Muscle strength assessment
Shall be done using Frankel scale

Full Information

First Posted
June 18, 2015
Last Updated
June 28, 2016
Sponsor
National Institute of Blood and Marrow Transplant (NIBMT), Pakistan
Collaborators
Armed Forces Institute of Regenerative Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02482194
Brief Title
Autologous Mesenchymal Stem Cells Transplantation for Spinal Cord Injury- A Phase I Clinical Study
Official Title
Autologous Transplantation of Bone Marrow Mesenchymal Stem Cells in Patients of Spinal Cord Injury-Phase I Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
March 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Blood and Marrow Transplant (NIBMT), Pakistan
Collaborators
Armed Forces Institute of Regenerative Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The conventional treatment of spinal cord injury (SCI) includes physical therapy and rehabilitation and in some cases may require surgical intervention. Although improved emergency care and aggressive treatment can help in preventing further damage and even restore minimal sensory functions, still a large proportion of patients suffer with prolonged disabilities. It led neurologists to search out for new treatment options for this otherwise debilitating disorder. Recent advances in research have developed a better understanding of stem cell biology especially their role in tissue repair and regeneration. Encouraging results in pre-clinical phase and limited human trials have proved that stem cells can be safely and effectively delivered to the injured site for regeneration of damaged tissue. Although a variety of cell types have been tried for their role in repair of spinal cord injury, majority of clinical trials employed stem cells taken from bone marrow especially mesenchymal stromal cells (MSC). Bone marrow MSCs are a good choice for regenerative therapies owing to advantages like ease of collection and ex-vivo culturing, immune tolerance and their ability to differentiate into a variety of cell types including neuronal lineage cells. Intravenous application or direct injection of MSCs into cerebrospinal fluid (CSF) via lumber puncture in animal models of SCI and brain trauma had shown that MSCs can migrate towards and integrate into injured spinal tissue and reduce cyst size and increase functional recovery. The literature indicates that acute, sub-acute and chronic injury can be a therapeutic target for MSC grafting. The mechanism of action may however vary among these conditions. In acute phase, MSC administration play anti-inflammatory role, while in sub-acute/chronic setting it may be used as neurostimulator and for cell bridging effect and possibly glial or neuronal cell replacement. The investigators propose a non-randomized, single group, open label, phase-I, interventional study to evaluate the safety and efficacy of intrathecal delivery of patient's own (autologous) bone marrow mesenchymal stem cells for treatment of spinal cord injury. This will include determination of functional recovery (neuro-muscular control and sensation) in the affected area and overall improvement in quality of life of the patients and also take into account any side effects, if observed.
Detailed Description
The role of regenerative therapies has gained more importance due to increased number of SCI in the wake of recent anti-terrorism operations by the armed forces and non-availability of any curative treatment for this category of patients. The promising results of preliminary clinical trials have proved that adult stem cells especially multipotent mesenchymal stromal cells can be safely injected and well tolerated and have shown functional improvement in SCI patients. The successful treatment in these patients will not only improve functional status of these otherwise debilitating patients, but can also reduce the burden on health care facilities. Mesenchymal stem cells have been shown to promote anatomical and functional recovery in animal models of SCI by promoting tissue sparing, axonal regeneration, and remyelination. Therapeutic effects of MSCs are primarily due to the secretion of soluble factors and the provision of extracellular matrix that provide protection and support repair. MSC are attractive candidates for transplantation into human patients because they can be easily harvested, expanded and banked, or derived directly from the patient allowing for autologous transplantation, obviating the need for immune suppression. In this study patients suffering from sub-acute and chronic phase of spinal cord injury shall be included. Patients will undergo detailed screening through MRI and motor and sensory assessment by ASIA score. Further evaluation will include electromyography (EMG) and tests for electroneurophysiological assessment like nerve conduction velocity (NCV) will also be done. Bone marrow aspiration will be done from iliac crest of the patients, followed by mononuclear cells (MNCs) separation by density gradient centrifugation. MNCs will be washed and cultured in tissue culture flasks. After 48 hours non-adherent cells will be removed from culture. Medium will be changed twice weekly till MSCs reach 70-80 % confluence. At that point MSCs will be harvested and after microbiological and other quality control testing the cellular preparation will be diluted to final concentration and infused by intrathecal injection. Primary outcome measure is safety which will be determined by clinical evaluation by two independent neurologists during one month of hospital stay after receiving treatment course. Secondary outcome measures will include American Spinal Injury Association (ASIA) impairment scale and NCV/EMG.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
Spinal cord injury, mesenchymal stem cells, transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Autologous mesenchymal stem cells
Arm Type
Experimental
Arm Description
use of mesenchymal stem cells as therapeutic intervention for spinal cord injury patients by autologous transplantation
Intervention Type
Biological
Intervention Name(s)
mesenchymal stem cells
Other Intervention Name(s)
MSC
Intervention Description
autologous transplantation of mesenchymal stem cells in spinal cord injury patients
Primary Outcome Measure Information:
Title
Number of adverse events
Description
Number of adverse events occurring in given time frame shall be reported to evaluate overall safety of the procedure
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Sensory and motor strength
Description
Improvement in sensitivity and motor strength will be measured through change in American Spinal Injury Association (ASIA) score from baseline
Time Frame
1 year
Title
Functional Independence
Description
Functional Independence will be measured by FIM scoring
Time Frame
1 year
Title
Muscle strength assessment
Description
Shall be done using Frankel scale
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients suffering from sub-acute and chronic phase of spinal cord injury Traumatic spinal cord injury at the thoracic level American Spinal Injury Association (ASIA) impairment scale "A" Confirmation by MRI of injury level Time between injury and enrollment greater than 2 weeks Ability to provide informed consent Exclusion Criteria: Axonic brain injury Inability to provide consent Open injuries Active infectious diseases Terminal patients Neurodegenerative diseases Evidence of meningitis Cerebral palsy Primary haematologic diseases Coagulopathies Pregnancy Other medical complications that contra-indicate surgery, including major respiratory complications Use of metal implants close to vascular structures (such as cardiac pacemaker or prosthesis) that contraindicate MRI.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Parvez Ahmed
Organizational Affiliation
Commandant Armed Forces Bone Marrow Transplant Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Armed Forces Bone Marrow Transplant Centre
City
Rawalpindi
ZIP/Postal Code
46000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
11922856
Citation
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Results Reference
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Citation
Zhang HT, Cheng HY, Cai YQ, Ma X, Liu WP, Yan ZJ, Jiang XD, Xu RX. Comparison of adult neurospheres derived from different origins for treatment of rat spinal cord injury. Neurosci Lett. 2009 Jul 24;458(3):116-21. doi: 10.1016/j.neulet.2009.04.045. Epub 2009 Apr 24.
Results Reference
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PubMed Identifier
20832402
Citation
Mackay-Sim A, St John JA. Olfactory ensheathing cells from the nose: clinical application in human spinal cord injuries. Exp Neurol. 2011 May;229(1):174-80. doi: 10.1016/j.expneurol.2010.08.025. Epub 2010 Sep 9.
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PubMed Identifier
21476980
Citation
Hernandez J, Torres-Espin A, Navarro X. Adult stem cell transplants for spinal cord injury repair: current state in preclinical research. Curr Stem Cell Res Ther. 2011 Sep;6(3):273-87. doi: 10.2174/157488811796575323.
Results Reference
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PubMed Identifier
20146557
Citation
Tetzlaff W, Okon EB, Karimi-Abdolrezaee S, Hill CE, Sparling JS, Plemel JR, Plunet WT, Tsai EC, Baptiste D, Smithson LJ, Kawaja MD, Fehlings MG, Kwon BK. A systematic review of cellular transplantation therapies for spinal cord injury. J Neurotrauma. 2011 Aug;28(8):1611-82. doi: 10.1089/neu.2009.1177. Epub 2010 Apr 20.
Results Reference
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PubMed Identifier
22464434
Citation
Karamouzian S, Nematollahi-Mahani SN, Nakhaee N, Eskandary H. Clinical safety and primary efficacy of bone marrow mesenchymal cell transplantation in subacute spinal cord injured patients. Clin Neurol Neurosurg. 2012 Sep;114(7):935-9. doi: 10.1016/j.clineuro.2012.02.003. Epub 2012 Mar 30.
Results Reference
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PubMed Identifier
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Citation
Dasari VR, Veeravalli KK, Dinh DH. Mesenchymal stem cells in the treatment of spinal cord injuries: A review. World J Stem Cells. 2014 Apr 26;6(2):120-33. doi: 10.4252/wjsc.v6.i2.120.
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Citation
All AH, Gharibani P, Gupta S, Bazley FA, Pashai N, Chou BK, Shah S, Resar LM, Cheng L, Gearhart JD, Kerr CL. Early intervention for spinal cord injury with human induced pluripotent stem cells oligodendrocyte progenitors. PLoS One. 2015 Jan 30;10(1):e0116933. doi: 10.1371/journal.pone.0116933. eCollection 2015.
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Citation
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Results Reference
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Autologous Mesenchymal Stem Cells Transplantation for Spinal Cord Injury- A Phase I Clinical Study

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