Stem Cells vs. Steroids for Discogenic Back Pain

Chronic Low Back Pain Clinical Trial

Official title:

Randomized, Comparative-effectiveness Study of Intradiscal Autologous Bone Marrow Concentrate Versus Intradiscal Corticosteroid for Chronic Discogenic Low Back Pain

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT04735185
• Other study ID #: IRB00250806
• Status: Suspended
• Phase: N/A
• Start date: September 30, 2025
• Est. completion date: November 30, 2028

Study information

• Verified date: October 2023
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized, comparative-effectiveness study comparing intradiscal autologous stem cells (from bone marrow aspirate) to intradiscal corticosteroid for the treatment of chronic discogenic low back pain (LBP). The primary objective of this study is to determine whether intradiscal autologous stem cells (from bone marrow aspirate) is more effective than intradiscal steroids for the treatment of chronic discogenic low back pain (LBP). Participants in this study will be randomized to receive up to intradiscal stem cell injections at 1 or 2 discs with cells harvested from a bone marrow aspirate drawn from participants' iliac crest, or an equal volume (2 mL) of intradiscal steroids and local anesthetic injected into the discs. In order to identify the painful disc(s), discography may be used at the discretion of the provider. Both treatments are frequently used as part of clinical care (i.e. there is no placebo group).

Description:

In this study, the investigators are attempting to determine if intradiscal injection of autologous bone marrow-derived mesenchymal stem cells (BMC) will decrease pain and improve function compared with intradiscal steroids.

Up to 106 patients with a clinical diagnosis of chronic discogenic low back pain for greater than 6 months, MRI evidence of lumbar disc degeneration limited to one or two discs with <50% disc height loss, and positive provocative discography (if clinically indicated) will be randomized to receive intradiscal BMC or steroid and long-acting local anesthetic (bupivacaine).

Those randomized to group I will receive a 2 mL intradiscal injection of autologous bone marrow-derived mesenchymal stem cells from bone marrow aspirate of the posterior ilium, while those randomized to group II will receive an intradiscal injection of the steroid methylprednisolone and the local anesthetic bupivacaine. The first follow-up will occur at 4-weeks post-treatment at which time rescue medications may be prescribed or adjusted but no other analgesic interventions should occur. The primary outcome measure will be pain relief at 3 months post-treatment, while a positive categorical outcome will be a 2-point or greater decrease in average LBP coupled with either a score > 5/7 on the PGIC (indicating noticeable improvement) or a 10-point decrease in ODI (indicating a clinically meaningful benefit). At 3 months, a repeat MRI will be obtained in selected patients at military treatment facilities (i.e. every 5th patient). Those who fail to experience a positive categorical outcome will be withdrawn from the study to receive alternate care, including an option for intradiscal BMC in those who received corticosteroid. For those who continue to experience a positive outcome, there will be 6- and 12-month follow up visits. At all follow-up visits, histories and physical exams will be performed and questionnaires assessing sleep, function, and anxiety and depression will be administered.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 106
• Est. completion date: November 30, 2028
• Est. primary completion date: November 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

1. Age = 18

2. Pain duration > 6 months

3. Failure of non-operative treatment > 3 months

4. Average pain score > 4/10 over the past week

5. Presumed clinical diagnosis of discogenic low back pain (such as back>leg pain, no or minimal radiation of pain past knee level, no significant improvement with epidural steroid injection, facet injections, sacroiliac joint injections and/or trigger point injections

6. Lumbar MRI within the last 18 months showing disc degeneration in <= 2 lumbar discs; <50% disc height loss in each disc

7. Patient agrees to have disc injection(s) and no other low back interventional or pharmacological treatments for at least 3 months

8. Patient agrees to be off all NSAIDs and corticosteroids from 2 weeks prior to and 3 months after the injection.

9. Stable dose of analgesic medications for at least 2 weeks

Exclusion Criteria:

1. Previous disc directed therapy involving heat (e.g. Intradiscal electrothermal therapy (IDET), biacuplasty)

2. Previous disc injection therapy in the last 3 months (e.g. corticosteroid, platelet rich plasma, stem cells)

3. Previous lumbar spine surgery (e.g. discectomy, fusion) at the affected levels (i.e. those with relief after surgery in whom adjacent segment discogenic pain is suspected can be considered on a case-by-case basis)

4. Disc extrusion or symptomatic disc protrusion at affected level

5. Untreated coagulopathy

6. Allergy to contrast dye or local anesthetics

7. Negative discography or discography showing > 2 positive discs

8. Pain > 15 years in duration

9. Opioid dose > 30 mg oral morphine equivalents per day (patients may be tapered down or off opioids)

10. Diffuse pain phenotype (e.g. diagnosis of fibromyalgia)

11. Secondary gain (e.g. ongoing medical board or litigation related to injury)

12. Pregnancy (study subject report of negative pregnancy status will be sufficient to participate. Testing will be provided if subject is unsure or requests a test to confirm.

13. Cannot read or understand English

Related Conditions & MeSH terms

• Back Pain
• Chronic Low Back Pain
• Degenerative Disc Disease
• Intervertebral Disc Degeneration
• Low Back Pain

Intervention

Other:
• Autologous stem cells
In this intervention participants will receive a 2 mL intradiscal injection into each affected disc of autologous bone marrow-derived mesenchymal stem cells from bone marrow aspirate of the posterior ilium.

Drug:
• Corticosteroid
In this intervention participants will receive a 1 mL intradiscal injection of the steroid methylprednisolone (40 mg/mL) into each affected disc.
• Local anesthetic
In this intervention participants will receive a 1 mL intradiscal injection of the local anesthetic bupivacaine 0.5% into each affected disc.

Locations

Country	Name	City	State
United States	Johns Hopkins Hospital	Baltimore	Maryland

Sponsors (3)

Lead Sponsor	Collaborator
Johns Hopkins University	The Geneva Foundation, United States Department of Defense

Country where clinical trial is conducted

United States, 

References & Publications (2)

Noriega DC, Ardura F, Hernandez-Ramajo R, Martin-Ferrero MA, Sanchez-Lite I, Toribio B, Alberca M, Garcia V, Moraleda JM, Sanchez A, Garcia-Sancho J. Intervertebral Disc Repair by Allogeneic Mesenchymal Bone Marrow Cells: A Randomized Controlled Trial. Transplantation. 2017 Aug;101(8):1945-1951. doi: 10.1097/TP.0000000000001484. — View Citation

Pettine KA, Murphy MB, Suzuki RK, Sand TT. Percutaneous injection of autologous bone marrow concentrate cells significantly reduces lumbar discogenic pain through 12 months. Stem Cells. 2015 Jan;33(1):146-56. doi: 10.1002/stem.1845. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean change in average low back pain score on 0-10 numerical rating scale	Mean change in average low back pain score over the past week at 3 months compared to baseline on 0-10 numerical rating scale (higher pain scores represent greater pain)	Baseline and 3 months
Secondary	Hospital Anxiety and Depression Scale score	14-question scale measuring anxiety and depression, with each question scored as 0-3 (higher numbers represent greater anxiety or depression).	4 weeks
Secondary	Hospital Anxiety and Depression Scale score	14-question scale measuring anxiety and depression, with each question scored as 0-3 (higher numbers represent greater anxiety or depression).	3 months
Secondary	Hospital Anxiety and Depression Scale score	14-question scale measuring anxiety and depression, with each question scored as 0-3 (higher numbers represent greater anxiety or depression).	6 months
Secondary	Hospital Anxiety and Depression Scale score	14-question scale measuring anxiety and depression, with each question scored as 0-3 (higher numbers represent greater anxiety or depression).	1 year
Secondary	Athens Insomnia Scale score	Scale measuring sleep dysfunction on an 8-question 0-24 scale, with higher numbers indicating greater dysfunction.	4 weeks
Secondary	Athens Insomnia Scale score	Scale measuring sleep dysfunction on an 8-question 0-24 scale, with higher numbers indicating greater dysfunction.	3 months
Secondary	Athens Insomnia Scale score	Scale measuring sleep dysfunction on an 8-question 0-24 scale, with higher numbers indicating greater dysfunction.	6 months
Secondary	Athens Insomnia Scale score	Scale measuring sleep dysfunction on an 8-question 0-24 scale, with higher numbers indicating greater dysfunction.	1 year
Secondary	Patient global impression of change (PGIC) score	1-7 scale evaluating, with higher scores indicating greater improvement.	4 weeks
Secondary	Patient global impression of change (PGIC) score	1-7 scale evaluating, with higher scores indicating greater improvement.	3 months
Secondary	Patient global impression of change (PGIC) score	1-7 scale evaluating, with higher scores indicating greater improvement.	6 months
Secondary	Patient global impression of change (PGIC) score	1-7 scale evaluating, with higher scores indicating greater improvement.	1 year
Secondary	Oswestry disability index score	0-100% score measuring function for back and/ leg pain (higher scores indicate worse function)	4 weeks
Secondary	Oswestry disability index score	0-100% score measuring function for back and/ leg pain (higher scores indicate worse function)	3 months
Secondary	Oswestry disability index score	0-100% score measuring function for back and/ leg pain (higher scores indicate worse function)	6 months
Secondary	Oswestry disability index score	0-100% score measuring function for back and/ leg pain (higher scores indicate worse function)	1 year
Secondary	Disc Degeneration based on MRI	Disc degeneration on MRI (graded as significantly improved, slightly improved, no change, and worsening degeneration, based on Pfirmann's scale).	3 months
Secondary	Average low back pain score on 0-10 numerical rating scale	Average low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	4 weeks
Secondary	Average low back pain score on 0-10 numerical rating scale	Average low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	3 months
Secondary	Average low back pain score on 0-10 numerical rating scale	Average low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	6 months
Secondary	Average low back pain score on 0-10 numerical rating scale	Average low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	1 year
Secondary	Mean change in worst low back pain score on 0-10 numerical rating scale	Mean change in worst low back pain score over the past week at week 4 compared to baseline on 0-10 numerical rating scale (higher pain scores represent greater pain).	Baseline and 4 weeks
Secondary	Mean change in worst low back pain score on 0-10 numerical rating scale	Mean change in worst low back pain score over the past week at week 3 months compared to baseline on 0-10 numerical rating scale (higher pain scores represent greater pain).	Baseline and 3 months
Secondary	Mean change in worst low back pain score on 0-10 numerical rating scale	Mean change in worst low back pain score over the past week at week 6 months compared to baseline on 0-10 numerical rating scale (higher pain scores represent greater pain).	Baseline and 6 months
Secondary	Mean change in worst low back pain score on 0-10 numerical rating scale	Mean change in worst low back pain score over the past week at week 1 year compared to baseline on 0-10 numerical rating scale (higher pain scores represent greater pain).	Baseline and 1 year
Secondary	Worst low back pain score on 0-10 numerical rating scale	Worst low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	4 weeks
Secondary	Worst low back pain score on 0-10 numerical rating scale	Worst low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	3 months
Secondary	Worst low back pain score on 0-10 numerical rating scale	Worst low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	6 months
Secondary	Worst low back pain score on 0-10 numerical rating scale	Worst low back pain score over the past week on 0-10 numerical rating scale (higher pain scores represent greater pain).	12 months
Secondary	Positive categorical outcome	Greater or equal to 2-point decrease in average low back pain score coupled with a PGIC score of 5 or higher or a decrease on Oswestry disability score of 10 or greater	4 weeks
Secondary	Positive categorical outcome	Greater or equal to 2-point decrease in average low back pain score coupled with a PGIC score of 5 or higher or a decrease on Oswestry disability score of 10 or greater	3 months
Secondary	Positive categorical outcome	Greater or equal to 2-point decrease in average low back pain score coupled with a PGIC score of 5 or higher or a decrease on Oswestry disability score of 10 or greater	6 months
Secondary	Positive categorical outcome	Greater or equal to 2-point decrease in average low back pain score coupled with a PGIC score of 5 or higher or a decrease on Oswestry disability score of 10 or greater	12 months