Skip to content

Comparison of efficacy of two types of different approaches for injection transformainal epidural space in lumber disc prolapse patient.

Comparison of clinical outcomes of lumbar transforaminal epidural steroid injection via the subpedicular (Safe Triangle) versus the Kambinâ??s Triangle approach in radicular pain with PIVD & spinal stenosis.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/07/020187
Enrollment
40
Registered
2019-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: lumbar transforaminal epidural steroid injection through subpdicular (Safe triangle) approach: single dose of 40 mg depot preparation of methyl prednisolone with 0.5ml Bupivacaine given

Sponsors

ESI Institute of Pain Management
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Presence of lumbar radicular pain with a pain intensity >= 4/10(NRS score) in a patient diagnosed with a herniated nucleus pulposus (HNP) or spinal stenosis (SS) after a series of physical, neurologic, and radiologic examinations & evidenced by lumbar spine magnetic resonance imaging (MRI). 2. No prior therapeutic TFESI within the previous 6 months . 3. No prior surgery .

Exclusion criteria

Exclusion criteria: 1. Generalized inflammatory diseases. 2. Previous use of anticoagulant agents. 3. Uncontrollable diabetes that could induce steroid adverse effects; 4. Previous adverse effects to lidocaine and/or contrast agents; 5. Current suspected or diagnosed infection. 6. Cutaneous disorders around the injection site, making it inappropriate for injecting agents . 7. Previous injection treatment at the same site within the past six months. 8. Patients with cauda equine syndrome. 9. Pregnancy & Cognitive impairment. 10. Patient Denial

Design outcomes

Primary

MeasureTime frame
Pain score in Neumeric Rating ScaleTimepoint: Before procedure, after 2 weeks and 4 weeks after procedure

Secondary

MeasureTime frame
Complications (spinal nerve pricking, discal injection, intrvascuar injection)Timepoint: Intra and post op period;Patient satisfaction with Macnabs CriteriaTimepoint: Before procedure, after 2 weeks and 4 weeks after procedure

Countries

India

Contacts

Public ContactDr Subrata Goswami

ESI Institute of Pain Management

drsgoswami@gmail.com09830430430

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026