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Treatment of Spinal Cord Injuries With (AutoBM-MSCs)vs (WJ-MSCs).

Assessment of Safety and Effectiveness of Mesenchymal Stem Cells in the Treatment of Spinal Cord Injury (SCI) Patients.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04288934
Enrollment
20
Registered
2020-02-28
Start date
2017-08-15
Completion date
2020-09-20
Last updated
2021-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injuries

Keywords

Spinal cord injuries, Mesenchymal Stem Cells, Allogenic, Bone marrow derived Mesenchymal stem cells, American Spinal Injury Association Impairment Scale

Brief summary

This study aims to assess and compare the safety and effectiveness of Autologous Bone Marrow-Derived MSCs (AutoBM-MSCs) in one group(group A) of SCI who are unlikely to be able to walk independently without treatment after 1 year of SCI, in the other group (group B) to assess the second group of Wharton Jelly derived mesenchymal stem cells ( WJ-MSCs) in the treatment of acute and subacute spinal cord injury (SCI) patients.

Detailed description

The study will be directed by the Cell Therapy Center (CTC) in Jordan, where 20 SCI patients meeting the inclusion criteria will be recruited and divided according to the type of injury into two groups; Group A for patients with complete transection of the spinal cord, and Group B for SCI without a total transaction,10 patients will receive (AutoBM-MSCs)and the other 10 patients with acute and subacute spinal cord injury will receive(WJ-MSCs) by a specialized spine surgeon into the spinal medulla. The outcomes and improvements will be assessed using the American Spinal Injury Association (ASIA) Impairment Scale (AIS) and the Spinal Cord Independence Measure (SCIM) version III, in addition to blood tests, MRI, and somatosensory evoked potential (SSEP).

Interventions

BIOLOGICALCollection and expansion of BM-MSC

MSCs collection from patients owns marrow using a volume of 20 ml of bone marrow obtained from iliac crest of SCI patients under local anesthesia. Manipulations of blood and bone marrow are to be done according to Good Laboratory Practice (GLP) using the gradient sedimentation method.

DIAGNOSTIC_TESTVI-SCI evaluation and patients' follow up

* At 6, and 12 months post MSCs transplantation, patients' spine will be imaged using 3 Tesla MRI and compared to baseline. * The (ASIA)/(ISNCSCI) score will be repeated every 3 months to evaluate any motor or neurological changes * The Spinal Cord Independence Measure (SCIM III) score will be repeated every 3 months to evaluate the effect on daily activities. * Blood samples will be withdrawn from patients at 3 months interval for biomarkers detection.

Sponsors

University of Jordan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Patients with complete transection of the spinal cord. Each group will then be subdivided into 2 subgroups with of 5 patients each; the 1st subgroup will be the patients with chronic SCI and the 2nd subgroup will be for the patients with subacute SCI.

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age: 18-70 years * Complete SCI grade AIS-A or -B, or incomplete C * SCI between cervical levels C5 and thoracic level T11 * At least 12 weeks since time of injury * Prediction rule score of 10 or less * Cognitively unaffected * Motivated for stem cell transplantation

Exclusion criteria

* Reduced cognition * Age under 18 years or above 70 years * Significant osteoporosis in spine and/or joints * Pregnancy (Adequate contraceptive use is required for women in fertile age) * Anoxic brain injury * Neurodegenerative diseases * Evidence of meningitis * Positive serology for HIV, HBV, HCV, or Syphilis. * Medical Complications that contraindicate surgery, including major respiratory complications. * Use of metal implants close to vascular structures (such as cardiac pacemaker or prosthesis) that contraindicate MRI. * Other medical conditions which can interfere with stem cell transplantation * Inability to provide informed consent. * Uncorrected vision * Cardiac abnormalities and uncontrolled hypertension

Design outcomes

Primary

MeasureTime frameDescription
SCI evaluation and patients follow up3 monthsthe (ASIA)/(ISNCSCI) to evaluate any motor or neurological changes, and the spinal cord independence measure (SCIM III) score to evaluate the effect on daily activities .these tests will be repeated every 3 months. blood samples will be withdrawn from patients as well to detect any biomarkers.
SCI evaluation and MSCs transplantation6-12 monthspost MSCs transplantation, patients' spine will be imaged using 3 Tesla MRI and compared to baseline.

Countries

Jordan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026