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Assessing the pain relief and recovery after giving steroid injection in spine for lower back pain due to nerve compression

A Prospective Observational study to assess the Functional Outcomes of Transforaminal Epidural Steroid Injection in Lumbar Radiculopathy - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112616
Enrollment
50
Registered
2026-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Transforaminal Epidural Steroid Injection: To evaluate the results of using 8 mg of dexamethasone sodium diphosph

Sponsors

Maharana Bhupal Government Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: clinical diagnosis of unilateral or bilateral lumbar radiculopathy with a positive single leg raise test MRI-confirmed lumbar disc herniation correlating with clinical symptoms failure of conservative management for more than or equal to two weeks that is rest, analgesics or physiotherapy vas score more than or equal to three

Exclusion criteria

Exclusion criteria: Patients with cauda equina syndrome Patients with motor weakness Patients presenting with classical foot drop Bladder and bowel involvement Previous lumbar spine surgery Spinal infections, malignancy, instability Contraindications to steroid injection e.g., active infection, uncontrolled diabetes, allergy to injectate Coagulopathy Pregnancy Patients with psychiatric symptoms and somatic pain syndrome

Design outcomes

Primary

MeasureTime frame
To measure the reduction in pain intensity following transforaminal epidural steroid injection using the Visual Numerical Scale (VNS) at predefined intervalsTimepoint: Immediately after inject, 1 week, 2 week, 1 month, 3 month

Secondary

MeasureTime frame
To assess the improvement in functional mobility by evaluating the change in Straight Leg Raise test valueTimepoint: immediately after the procedure;To determine the patient-reported satisfaction with the procedureTimepoint: 1 week, 2-week, 1 month and 3 months;To document any procedure-related complications or adverse eventsTimepoint: till 3 months after procedure

Countries

India

Contacts

Public ContactDr Khemraj Meena

R.N.T. Medical College

Khemraj10@gmail.com9414759782

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026