Skip to content

RCT ON CAUDAL EPIDURAL STEROID INJECTION AND NCV OUTCOME IN LUMBOSACRAL RADICULOPATHY

EFFECT OF CAUDAL EPIDURAL STEROID INJECTION ON ELECTRODIAGNOSTIC PARAMETERS IN PATIENTS WITH LUMBOSACRAL RADICULOPATHY: A DOUBLE BLINDED RANDOMISED CONTROLLED TRIAL - ECESIEP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033709
Enrollment
40
Registered
2021-05-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: G55- Nerve root and plexus compressionsin diseases classified elsewhere

Interventions

Intervention1: Standard treatment caudal epidural steroid injection STCESI group: 1ml of Corticosteroid (40mg Triamcinolone) plus 19 ml normal saline injected into caudal epidural space under USG guid

Sponsors

AIIMS Raipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1: Patients with lower back pain with unilateral or bilateral radiculopathy of minimum one month’s duration. 2: Physical examination should show radicular irritation or abnormalities in the sensory, motor, and/or reflex of the lower lumbar or upper sacral nerve root distribution 2: Both sex and all adults (above 18 years) will be included 3: Patients with MRI findings of disc protrusion or disc bulge at multiple levels of lumbosacral spine showing nerve impingement of lower lumbar or upper sacral roots with or without canal stenosis.

Exclusion criteria

Exclusion criteria: 1: Patients with severe psychiatric illness or any disease precluding prone positioning for the injection procedure. 2: Patients with active infections or otherwise severely ill with any co morbid condition. 3: Patients with neurological involvement that mandates immediate surgical interventions like cauda equina symptoms or bladder bowel incontinence. 4: Patients having bleeding disorders and with history of allergy to local anesthetics.

Design outcomes

Primary

MeasureTime frame
1.Numerical rating scale 2.Oswestry Low Back Pain Disability IndexTimepoint: Two weeks

Secondary

MeasureTime frame
NCV of lower extremities ( including CMAP, f wave of common peroneal, posterior tibial nerve and h reflex)Timepoint: Two weeks

Countries

India

Contacts

Public ContactDr Jaydeep Nandi

AIIMS Raipur

jaydeepnandidgp@gmail.com09760456198

Outcome results

None listed

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