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Multiple sclerosis is a multifocal inflammatory disease of the central nervous system which affects young individuals and causes paralysis of the limbs, sensation, visual and sphincter problems. The disease is caused by an autoimmune mechanism, ie the immune system produces antibodies and cells which attack the self myelin antigens, causing therefore demyelination. The disease is clinically evident with relapses of neurological disability due to the dysfunction of the areas (plaques of multiple sclerosis) in which damage of myelin occurs. Disability can accumulate with time and the disease enters a progressive phase due to damage of the axons and irreversible neurodegeneration. Although, effective immunotherapies exist which downregulate the autoimmune anti-myelin reactivity and reduce the rate of relapses of MS (like Copaxone and interferons), there is no effective means today to stop the progression of disability and induce rebuilding of the destroyed myelin.Adult bone marrow derived stromal cells (MSC) were shown to induce similar (to the neuronal stem cells) immunomodulatory and neuroregenerative effects and were shown in our laboratory to induce neuroprotection in the animal model of chronic experimental autoimmune encephalomyelitis (EAE). These bone marrow derived MSCs offer practical advantages for clinical therapeutic applications, since they can be obtained from the adult bone marrow and therefore the patient can be the donor for himself, without any danger for rejection of the cells. In addition, MSCs carry a safer profile and are less prone to malignant transformation.
Our center will perform a clinical trial with intra venous transplantation of bone marrow derived mesenchymal stem cell.our purpose is to evaluate the safety and feasibility of cell transplantation after 1year following up.
In the clinical trial 30 patients with multiple sclerosis who are drug resistance will take apart.Based on inclusion and exclusion criteria patients are chosen.Bone marrow aspiration will be done for all of them under local anesthesia.Patients are randomly divided in 2 groups:case and control. Then mesenchymal stem cells which are separated and prepared will be transplanted by intravenous injection to the patients in case group and the cells which obtain from patients in control group are frozen and inject after 6 months. Patients will be followed by Evaluation of EDSS MSFC RAO Test brain and cervical MRI and quality of life questionnaire after 1th 3th 6th and 12th months after transplantation.all these tests will be done before transplantation as basic evaluation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| cell free media | Placebo Comparator | 15 patients with relapsing remitting multiple sclerosis who receive cell free media |
|
| mesenchymal stem cell reciepiants | Experimental | Patients with relapsing remitting multiple sclerosis who underwent intravenous injection of mesenchymal stem cells |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| intravenous injection of mesenchymal stem cells | Biological | 15 patients with relapsing remitting multiple sclerosis underwent intravenous injection of mesenchymal stem cell |
|
| Measure | Description | Time Frame |
|---|---|---|
| MRI metrics changes | evaluate the effect of mesenchymal stem cell transplantation on number of GD positive lesions. | 6 months |
| Brain atrophy | evaluate the effect of mesenchymal stem cell transplantation to improve brain atrophy | 12 months |
| number of sever relapses | evaluation the effect of mesenchymal stem cell transplantation on number of sever relapses | 6 months |
| EDSS | Evaluation the effect of mesenchymal stem cells on progression of disease based on EDSS | 6 months |
| MSFC | Evaluation the effect of mesenchymal stem cells transplantation on MSFC | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| quality of life | Evaluation the effect of mesenchymal stem cell transplantation on patients quality of life | 6 months |
| RAO Test | Evaluation the effect of mesenchymal stem cell transplantation on RAO Test. |
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Inclusion Criteria:
Both gender
Age: 18-55years
Duration of disease: 2-10 years
Relapsing remitting with drug resistance
EDSS: 3-6.5
Resistance to immunomodulatory and cytotoxic drugs:
Secondary progressive or relapsing multiple sclerosis
Primary progressive MS with relapse or GAD positive enhancement
Secondary progressive MS with relapse
Secondary progressive MS without relapse:progression of disease with 1 point increase of EDSS during last 18 months
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Hamid Gourabi, PhD | head of Royan Institute | Study Chair |
| Nasser Aghdami, MD,PhD | Head of cell therapy center of Royan Institute | Study Director |
| Masoud Nabavi, MD | scientist and clinician | Principal Investigator |
| Leila Arab, MD | Department of regenerative medicine,Royan Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Royan Institute | Tehran | Iran |
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| Label | URL |
|---|---|
| Related Info | View source |
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| ID | Term |
|---|---|
| D009103 | Multiple Sclerosis |
| ID | Term |
|---|---|
| D020278 | Demyelinating Autoimmune Diseases, CNS |
| D020274 | Autoimmune Diseases of the Nervous System |
| D009422 | Nervous System Diseases |
| D003711 | Demyelinating Diseases |
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| ID | Term |
|---|---|
| D033581 | Stem Cell Transplantation |
| D035061 | Control Groups |
| ID | Term |
|---|---|
| D017690 | Cell Transplantation |
| D064987 | Cell- and Tissue-Based Therapy |
| D001691 | Biological Therapy |
| D013812 | Therapeutics |
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|
| injection of cell free media | Biological | Patients who are in control group underwent media injection but after 6 months they will be transplanted by stem cell. |
|
|
| 6 months |
| intravenous cell transplantation | evaluation the side effect of intravenous transplantation of mesenchymal stem cell | 6 months |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
| D014180 |
| Transplantation |
| D013514 | Surgical Procedures, Operative |
| D015340 | Epidemiologic Research Design |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D012107 | Research Design |
| D008722 | Methods |