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Transforaminal Intradiscal Steroid Injection and Epidural Steroid Injection for the Treatment of Chronic Low Back Pain: A Prospective, Randomized, Controlled Study

The Clinical Study on Transforaminal Intradiscal Steroid Injection and Epidural Steroid Injection in the Treatment of Chronic Low Back Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096006
Enrollment
Unknown
Registered
2025-01-16
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Chronic discogenic low back pain

Interventions

Trial group:transforaminal intradiscal steroid injection (Transforaminal Intradiscal Steroid Injection, TISI)
Control group:transforaminal epidural steroid injection (Transforaminal Epidural Steroid Injection, TESI)

Sponsors

Beijing Shijitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 70 years (2) Duration of low back pain exceeding 3 months (3) Numerical Rating Scale (NRS) >=4. (4) Failure of at least 3 months of standard conservative treatment. (5) Diagnosed as lumbar discogenic low back pain through physical examination and imaging, with MRI showing Modic?changes in the affected disc. (6) No similar injection treatments received within the past 6 months.

Exclusion criteria

Exclusion criteria: (1) Severe spinal deformities, trauma, fractures, lumbar myofascial pain syndrome, lumbar spinal stenosis, lumbar spondylolisthesis, spinal tumors, spinal infections, or inflammatory diseases (2) Pregnancy (3) Allergy to steroids or contrast agents (4) Systemic infectious diseases or localized skin infections at the puncture site (5) Previous interventional procedures or surgeries on the same segment of the intervertebral disc (6) Severe coagulation dysfunction (7) Modic ? changes in multiple lumbar levels of intervertebral disc degeneraton (8) Comorbidity with psychiatric disorders that may impair cooperation (9) Refusal to sign the informed consent form

Design outcomes

Primary

MeasureTime frame
Low back pain condition;

Secondary

MeasureTime frame
Function of the lumbar Spine;Functional disability caused by low back pain;Quality of life;Psychiatric status assessment;Intervertebral disc calcification;Intervertebral disc height;Degenerative changes of the intervertebral disc;

Countries

China

Contacts

Public ContactJipeng Song

Beijing Shijitan Hospital, Capital Medical University

sjpfly@163.com+86 158 0169 0753

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 26, 2026