Allogeneic BM-MSCs in Patients with Lumbar Facet Arthropathy

Mayo Clinic10 enrolled

Overview

Researchers are conducting this study to learn more about the side effects of bone marrow-derived stem cells when injected into the facet joints for the treatment of painful lumbar facet joint arthropathies.

Phase I prospective study to determine the safety and feasibility of allogeneic, culture-expanded BM-MSCs in subjects with painful facet-mediated low back pain. Target accrual is 10 subjects with diagnosis of painful lumbar facet joint arthropathy. Eligible subjects will receive a single set of intra-articular bilateral injections of allogeneic, culture-expanded BM-MSCs human, allogeneic, culture expanded, bone-marrow-derived mesenchymal stem cells. Subjects will be evaluated at baseline, treatment day 0, post-operative day 1, post-operative days 3-5, week 2, and months 3, 6, 12, 18 and 24 months post-treatment.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Facet-Mediated Low Back Pain

Interventions

Single bilateral intra-articular injection of allogeneic BM-MSCs for lumbar facet joint arthropathyDRUG

Single bilateral intra-articular injection of manufactured cell cultured expanded allogeneic BM-MSCs for painful lumbar facet joint arthropathy

Eligibility

Sex: ALLMin age: 40 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: Male or female subjects ages 40-70 years who fulfill the following criteria: 1. Persons of childbearing potential must be non-nursing and have a negative serum pregnancy test to be included in the trial and will agree to use adequate contraception (hormonal or barrier method or abstinence) from the time of screening to a period of 24 months following completion of the drug treatment cycle. 2. Clinical diagnosis of symptomatic facet joint arthropathy involving the L3-S1 facets. 3. Radiographic evidence of facet arthropathy involving the L3-S1 facets. 4. Chronic low back pain with or without referred pain to the buttock, groin, or proximal thigh. 5. Confirmation of facet joint related pain by medial branch block with positive results. 6. Full understanding of the requirements of the study and willingness to comply with the treatment plan, including laboratory tests, diagnostic imaging, and follow-up visits and assessments. 7. Can provide written informed consent. Exclusion Criteria: 1. Extreme obesity, as defined by NIH Clinical Guidelines Body Mass Index (BMI \> 40) 2. Subjects who are pregnant or nursing or subjects planning to become pregnant in the first 24 months post-treatment. 3. Subjects with current or prior history of spinal infection at the symptomatic level. 4. Subjects with a diagnosis of severe osteoporosis with pathological fracture. 5. Radiofrequency ablation at the index level prior to injection in the past 3 months with positive results. 6. Any lumbar facet intra-articular injection including steroids at the index facet level prior to treatment injection in the past 3 months 7. Subjects that have undergone a procedure affecting the structure/biomechanics of the index facet joint or a spinal fusion adjacent to the symptomatic level. 8. Have undergone any procedure using biological treatment for any condition such as bone marrow aspirate concentrate, PRP, bone marrow-derived MSCs, adipose-derived MSCs, SVF, micro fragmented fat, embryonic membrane product etc. 9. Clinically relevant instability on flexion-extension as determined by the primary investigator by overlaying films. 10. Have an acute fracture of the spine at the time of enrollment in the study or clinically compromised vertebral bodies at the affected level due to current or past trauma. 11. Presence of any of the following spinal deformities: spondylolysis at the corresponding facet level, spondylolisthesis \> grade II at the index facet. 12. Epidural steroid injections within 4 weeks prior to treatment injection. 13. Active malignancy or tumor as a source of symptoms or history of malignancy within the 5 years prior to enrollment in the study, except history of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or squamous cell carcinoma of the cervix if fully excised and with clear margins. 14. An elevated average baseline morphine equivalent dose, as determined by the investigator during screening consultation. 15. Taking systemic immunosuppressant medications or having a chronic, immunosuppressive state. 16. Taking anti-rheumatic disease medication (including methotrexate or other antimetabolites) within 3 months prior to study enrollment. 17. Clinically significant abnormal hematology. 18. Ongoing infectious disease, including but not limited to tuberculosis, HIV, hepatitis, and syphilis. 19. Unexplained fever, defined as greater than 100.4 degrees Fahrenheit or 38.0 degrees Celsius, or mental confusion at baseline. 20. Clinically significant cardiovascular, neurological, renal, hepatic or endocrine disease. 21. Participation in a study of an experimental drug or medical device for treatment of facet joint arthropathy within one year. 22. Any contraindication to MRI according to MRI guidelines or unwillingness to undergo fluoroscopic procedures. 23. History of or current evidence of alcohol or drug abuse or dependence, recreational use of illicit drug or prescription medications, or medical marijuana 24. Any illness or condition which, in the investigators' judgment will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results. 25. Being involved in active litigation related to subject's low back pain. 26. Have a mental illness that could prevent completion of the study or protocol questionnaires.

Locations (1)

Mayo Clinic in Florida

Jacksonville, Florida, United States

Outcomes

Primary Outcomes

Clinical assessment of nature, incidence, and severity of adverse events (AEs)

Clinical examination face-to-face during follow-up visits

Time frame: 24 months

Self-reported assessment of nature, incidence, and severity of AEs

Spontaneous subject reports

Time frame: 24 months

Study personnel assessment of nature, incidence, and severity of AEs

Subject interview by study personnel

Time frame: 24 months

Secondary Outcomes

Global Health Scale (GHS)

Self-reported questionnaire to assess an individual's physical, mental, and social health. Standardized response scores ranges vary from1 to 5 (e.g., 1= None to 5=Very severe) or reversed (5=None to 1=Very severe) to ensure that higher scores for responses always indicate better health.

Time frame: 24 months

Visual Analog Scale (VAS) - back and leg pain

Subjective self-reported scale (1-10) to measure acute and chronic pain. (0= no pain; 10= worst pain possible).

Time frame: 24 months

Oswestry Disability Index (ODI)

Self-reported index to quantify disability for low back pain. Scores vary from 0 (no back pain) to 5 (worst back pain) in 10 sections (pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sex life, social life, and traveling). ODI Index is calculate.

Time frame: 24 months

Patient Health Questionnaire-4 (PHQ-4)

Self-reported brief questionnaire to screen for anxiety and depression. Four questions scoring 0 (not at all) to 3 (nearly every day).

Data from ClinicalTrials.gov

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