Transplantation of Autologous Olfactory Ensheathing Cells in Complete Human Spinal Cord Injury
Primary Purpose
Complete Spinal Cord Injuries
Status
Unknown status
Phase
Phase 1
Locations
Poland
Study Type
Interventional
Intervention
olfactory mucosa ensheathing cell grafting, rehabilitation
rehabilitation
Sponsored by
About this trial
This is an interventional treatment trial for Complete Spinal Cord Injuries focused on measuring human, spinal cord injury, olfactory ensheathing cells, transplantation
Eligibility Criteria
Inclusion Criteria:
- spinal cord injury at subacute or chronic stage
- a single spinal cord injury between segments C5 and L5
- myelopathy confirmed by MRI, not exceeding 2 spinal cord segments
- loss of sensory and motor function below the injury, confirmed in control studies (ASIA Category A)
- age from 16 to 65 years
- patient undergoing continuous rehabilitation
- good patient motivation and cooperation
- signed informed consent
Exclusion Criteria:
- a coexisting lesion of the nervous system
- progressive post-traumatic syringomyelia
- significant spinal stenosis or instability
- persistent neuropathic pain
- muscle atrophy or joint ossifications
- severe systemic disease (neoplasm, contagious disease, diabetes etc.)
- chronic sinusitis
- tumors or polyps of nasal cavities
- persistent hyposmia or anosmia
- pregnant or breastfeeding women
Sites / Locations
- Department of Neurosurgery of Wroclaw Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
olfactory ensheathing cell recipient
control
Arm Description
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT01231893
First Posted
October 29, 2010
Last Updated
October 29, 2010
Sponsor
Wroclaw Medical University
Collaborators
Institute of Immunology and Experimental Therapy of the Polish Academy of Sciences, Department of Rehabilitation in Spinal Cord Injuries Akson
1. Study Identification
Unique Protocol Identification Number
NCT01231893
Brief Title
Transplantation of Autologous Olfactory Ensheathing Cells in Complete Human Spinal Cord Injury
Official Title
Transplantation of Autologous Olfactory Ensheathing Cells for Treatment of Complete Human Spinal Cord Injuries- a Phase I Clinical Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2010
Overall Recruitment Status
Unknown status
Study Start Date
May 2008 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Wroclaw Medical University
Collaborators
Institute of Immunology and Experimental Therapy of the Polish Academy of Sciences, Department of Rehabilitation in Spinal Cord Injuries Akson
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this experimental therapy is an assessment of the safety and feasibility of transplantation of autologous olfactory ensheathing glia and olfactory fibroblasts obtained from the olfactory mucosa in patients with complete spinal cord injury.
Detailed Description
The increasing number of patients (mostly young), who have sustained a spinal cord injury mainly as a result of motor vehicle accidents, falls or violence has become worldwide a serious clinical, social and economical problem. Most accepted treatment protocols for spinal cord injury focus on techniques of early neuro-protection aimed at maximal prevention of secondary spinal cord injury (administration of methylprednisolon and spinal cord surgical decompression) as well as on methods of stimulation of plasticity in the central nervous system (neurorehabilitation). While these methods have been shown to stimulate functional recovery in patients with incomplete spinal cord injury, the results of treatment of patients with severe incomplete and complete spinal cord injuries remain unsatisfactory. This is due to the lack of spontaneous regeneration of lesioned axons in the spinal cord. Results from a substantial number of animal experiments performed mainly on the model of mammalian spinal cord injury in the last 3 decades led to the establishment of numerous regeneration-promoting strategies including application of neurotrophic factors, antibodies blocking the myelin-associated proteins and transplantation of cells with neurotrophic activity. Olfactory ensheathing cells (OECs) are an unique population of macroglia found in the lamina propria of olfactory mucosa, around the olfactory nerve fascicles and in the two outer layers of the olfactory bulb. These cells have the natural ability to stimulate the regrowth of lesioned peripheral and central axons. In a Phase I non-randomized controlled prospective study we have tested the hypothesis that a combined approach for treatment of complete spinal cord injuries consisting of intraspinal transplantation of a mixture of autologous OECs and fibroblasts isolated from the olfactory mucosa, combined with intense neuro-rehabilitation is safe and feasible.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Complete Spinal Cord Injuries
Keywords
human, spinal cord injury, olfactory ensheathing cells, transplantation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
olfactory ensheathing cell recipient
Arm Type
Experimental
Arm Title
control
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
olfactory mucosa ensheathing cell grafting, rehabilitation
Intervention Description
In this group patients are planned to underwent a biopsy of their own olfactory mucosa for isolation and culture of olfactory ensheathing cells and olfactory fibroblasts. The suspension of these cells will be next transplanted into the focus of spinal cord injury. Before and after surgery the patients will undergo an intense neurorehabilitation program.
Intervention Type
Other
Intervention Name(s)
rehabilitation
Intervention Description
In this group the patients will not undergo any surgical procedure. They will participate in the same rehabilitation protocol that is planned for the patients from the experimental group.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
spinal cord injury at subacute or chronic stage
a single spinal cord injury between segments C5 and L5
myelopathy confirmed by MRI, not exceeding 2 spinal cord segments
loss of sensory and motor function below the injury, confirmed in control studies (ASIA Category A)
age from 16 to 65 years
patient undergoing continuous rehabilitation
good patient motivation and cooperation
signed informed consent
Exclusion Criteria:
a coexisting lesion of the nervous system
progressive post-traumatic syringomyelia
significant spinal stenosis or instability
persistent neuropathic pain
muscle atrophy or joint ossifications
severe systemic disease (neoplasm, contagious disease, diabetes etc.)
chronic sinusitis
tumors or polyps of nasal cavities
persistent hyposmia or anosmia
pregnant or breastfeeding women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pawel Tabakow, M.D. Ph.D.
Phone
48 606 137 846
Email
p.tabakov@wp.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Wlodzimierz Jarmundowicz, M.D. Ph.D.
Phone
48 601 706 816
Email
jarmund@wp.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wlodzimierz Jarmundowicz, M.D. Ph.D.
Organizational Affiliation
Department of Neurosurgery of Wroclaw Medical University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Pawel Tabakow, M.D. Ph.D.
Organizational Affiliation
Department of Neurosurgery of Wroclaw Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurosurgery of Wroclaw Medical University
City
Wroclaw
ZIP/Postal Code
50-556
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pawel Tabakow, M.D. Ph.D.
First Name & Middle Initial & Last Name & Degree
Wlodzimierz Jarmundowicz, M.D. Ph.D.
First Name & Middle Initial & Last Name & Degree
Bogdan Czapiga, M.D. Ph.D.
First Name & Middle Initial & Last Name & Degree
Ryszard Miedzybrodzki, M.D. Ph.D.
First Name & Middle Initial & Last Name & Degree
Wojciech Fortuna, M.D. Ph. D.
First Name & Middle Initial & Last Name & Degree
Marcin Czyz, M. D. Ph. D.
First Name & Middle Initial & Last Name & Degree
Dariusz Szarek, M.D.
First Name & Middle Initial & Last Name & Degree
Stefan Okurowski, MPT
First Name & Middle Initial & Last Name & Degree
Juliusz Huber, M.D. Ph. D.
First Name & Middle Initial & Last Name & Degree
Pawel Szewczyk, M.D.
12. IPD Sharing Statement
Links:
URL
http://www.sci-therapies.info
Description
Related Info
Learn more about this trial
Transplantation of Autologous Olfactory Ensheathing Cells in Complete Human Spinal Cord Injury
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