Lumbar Disc Herniation Clinical Trial
Official title:
Safety and Effectiveness of Human Umbilical Cord Mesenchymal Stem Cells For the Treatment of Lumbar Disc Degeneration Disease
NCT number | NCT04414592 |
Other study ID # | QFu |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2020 |
Est. completion date | March 2023 |
This study aims to investigate the safety and efficiency of Human Umbilical Cord Mesenchymal Stem Cells (hUCMSC) for treating lumbar disc degeneration diseases. We hypothesize grafting hUCMSC into the degenerative disc leads to symptoms relief and slow down the progression of disc degeneration.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | March 2023 |
Est. primary completion date | March 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. Age: 18-60 years old; 2. Symptoms with lower back pain and unilateral radicular pain; 3. Failure of conservative treatments including physical therapy, manipulation therapy and non-morphine drug therapy; 4. CT/MRI clearly showing unilateral nucleus pulposus herniation to compress the nerve root; 5. Symptoms and imaging showing unilateral lumbar disc herniation; 6. Imaging showed single-segment lumbar disc herniation; 7. Pfirrmann disc degeneration classification from lumbar MRI: grade I-IV; 8. Segments of lumbar disc herniation: L3-4, L4-5, L5-S1; 9. Unilateral full endoscopic lumbar discectomy; 10. Signing the informed consent; 11. No previous history of spinal surgery. Exclusion Criteria: 1. Previous history of tumor or spinal infection; 2. Severe coagulation disorders or are taking oral anticoagulants 3. coma or incapacity; 4. MRI contraindications (cardiovascular and cerebrovascular stent implantation history, cardiac pacemaker, biological stimulator, etc.); 5. pregnant; 6. pregnancy or breastfeeding; 7. participated in other clinical trials in the past 30 days; 8. History of stem cell therapy; 9. poor compliance, or inability to properly understand the coordination; 10. received intervertebral disc interventional therapy, such as radiofrequency, laser ablation, protease injection and ozone injection in the past 3 months; 11. Highly allergic constitution or severe allergic history; 12. Severe autoimmune diseases or receiving immunosuppressive therapy; 13. Severe infection or high fever; 14. Shock, failure of vital organs or unstable vital signs; 15. X-ray showing that the stenosis percentage of the degenerative segment was larger than 30% compared to that of the adjacent normal segment. 16. Lumbar disc herniation with calcification; 17. Lumbar disc herniation with Modic Change; 18. Lumbar disc herniation with severe spinal stenosis; 19. Lumbar disc herniation with lumbar spondylolisthesis; 20. Lumbar disc herniation with spinal deformity; 21. psychosocial abnormalities, cognitive impairment, or other physical diseases affecting the research results; 22. Other reasons. |
Country | Name | City | State |
---|---|---|---|
China | Shanghai General Hospital | Shanghai | Shanghai |
China | Shanghai General Hospital | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine |
China,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Lumbar disc signaling values from magnetic resonance imaging | Changes from baseline in Lumbar disc signaling values from magnetic resonance imaging | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | Visual Analogue Scale (VAS) (0-10 scores, the higher scores mean a worse outcome) | Changes from baseline in Visual Analogue Scale of Lower back pain and leg pain | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | Oswestry Disability Index(ODI) (0-50 scores, the higher scores mean a worse outcome) | Changes from baseline in Oswestry Disability Index | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | The Short Form (36) Health survey (SF36) (0-100 scores, the higher scores mean a better outcome) | Changes from baseline in The Short Form (36) Health survey (SF36) | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | Disc Height Index (DHI) from X ray | Changes from baseline in Disc Height Index | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | Size of herniated nucleus pulposus from magnetic resonance imaging | Changes from baseline in size of nucleus pulposus from magnetic resonance imaging | Baseline, post-op 3months, post-op 6months, post-op 12months | |
Secondary | Number of participants with treatment-related adverse events by CTCAE v4.0 | Assessing for worsening of patients' baseline symptoms or functions (will be considered an AE); (also general AE events), particular AE events related to the procedures/treatment. All AEs will be assessed by common terminology criteria for adverse events. | From baseline until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months |
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