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Evaluation of Transforaminal Epidural Steroid Injection in Radicular Low Back Pain According to MSU Classification

Not Applicable
Completed
Conditions
Disc Herniation
Low Back Pain
Radiculopathy Lumbar
Injections, Epidural
Interventions
Procedure: Transforaminal Epidural Steroid Injection
Registration Number
NCT06275529
Lead Sponsor
Başakşehir Çam & Sakura City Hospital
Brief Summary

Low back pain is a common disease in all ages and it effects seriously quality of life. Medical treatment,interventional methods and surgery are the treatment options. Transforaminal epidural steroid injections (TFSI) is one of the interventional method for radiculopathy with low back pain. Michigan State University(MSU) classification is a MRI based disc herniation classification. It helps to classified disc herniation in types, places and sizes.

The aim of this study to evaluate the pain and oswestry disability index in patients who have radiculopathy with low back pain, undergone TFSI according to MSU classification.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
160
Inclusion Criteria
  • between the ages of 18-65
  • After outpatient evaluation, a decision was made to perform transforaminal steroid injection,
  • Low back pain of more than 6 on a numeric rating scale (NRS)
  • Radiculopathy for more than 4 weeks and less than one year and straight leg raising <45
  • Disc herniation at the L4-L5 or L5-S1 level on MRI
  • Failure to respond to medical treatment for at least one month
Exclusion Criteria
  • Neurological deficit,
  • Bleeding problems,
  • Localized infection,
  • Spinal pathologies (such as tumors),
  • Fractures,
  • Severe stenosis,
  • Uncontrolled diabetes,
  • Pregnancy,
  • Red flag symptoms (such as motor and/or sphincter dysfunction)
  • Patient reluctance,
  • Computed tomography (CT) and MRI findings in favor of sequestrated fragments from herniated disc,
  • Sphincteric disorders,
  • Previous spine surgeries

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MSU Classification 3ATransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 3A
MSU Classification 2ABTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 2AB
MSU Classification 1CTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 1C
MSU Classification 2ATransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 2A
MSU Classification 2BTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 2B
MSU Classification 3BTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 3B
MSU Classification 1BTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 1B
MSU Classification 3ABTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 3AB
MSU Classification 1ATransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 1A
MSU Classification 2CTransforaminal Epidural Steroid InjectionTransforaminal Epidural Steroid Injection, MSU classification according to MRI images 2C
Primary Outcome Measures
NameTimeMethod
Change of the disability scorePre-intervention, post-intervention 1th month and post-intervention 3rd month

Disability conditions of the patients are assessed by using "Oswestry Disability Index" (ODI). ODI is a patient completed questionnaire which gives a percentage score of disability. The ODI is comprised of 10 items and enquires about functional limitations in various activities of daily living with the index score ranging from 1 (best) to 100 (worst).

The change in ODI scores between the ten groups will be compared.

Change of the pain severity scorePre-intervention, post-intervention 1th month and post-intervention 3rd month

Pain severity is assessed by using "Numeric Rating Scale" (NRS). Patients give score of their pain between 0 (no pain) and 10 (worst possible pain).

The change in NRS scores between the ten groups will be compared.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Başakşehir Çam and Sakura City Hospital

🇹🇷

İstanbul, Turkey

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