Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
ID06092749

Effectiveness of Transgrade vs Interlaminar Epidural Steroid Injection for Chronic Unilateral Lumbar Radicular Pain

Led by Ain Shams University · Updated on 2026-04-01

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic neuropathic lumbar pain is a common and challenging condition affecting many patients, often causing persistent leg and back pain. This trial compares two approaches for managing this pain: Transgrade (TG) epidural steroid injection, a new technique using a special angled needle without extra equipment, and Interlaminar (IL) epidural steroid injection, which delivers medication between adjacent vertebrae. The study aims to evaluate which method provides better pain relief for people who have not responded well to conventional treatments. Participants will be randomly assigned to receive either the Transgrade or Interlaminar epidural steroid injection. Both procedures involve delivering steroid medication into the epidural space of the lower spine but use different needle techniques. The study is double-blinded, meaning neither participants nor researchers will know which treatment is given. The primary outcome is the number of patients experiencing successful pain relief measured at three months after the intervention, with follow-up extending to six months. During the study, participants will be monitored regularly to assess pain relief and any side effects. Pain intensity will be measured using a numeric rating scale, and medical evaluations will ensure ongoing safety. Participants must have a history of persistent unilateral leg and back pain for more than six months and an unsatisfactory response to standard therapies. The total study period includes treatment and follow-up visits over six months to gather comprehensive data on treatment effectiveness and safety.

CONDITIONS

Brief Title

Chronic Unilateral Lumbar Radicular Pain

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Persistent pain in one leg with back pain lasting more than 6 months
  • Age 21 years or older
  • Able to give informed consent
  • Unsatisfactory response to conventional treatments including physical therapy or medications with a numeric rating scale (NRS) score of 5 or higher
Not Eligible

You will not qualify if you...

  • Previous lumbar spinal surgery
  • Presence of myelopathy
  • Rheumatoid disorders
  • Psychiatric disorders
  • Bleeding or coagulation disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single intervention with follow-up through 6 months post-intervention

Participants receive either the Transgrade or Interlaminar Epidural Steroid Injection technique for chronic unilateral lumbar radicular pain.

1 intervention visit and follow-up assessments up to 6 months

Trial Site Locations

Total: 1 location

1

Ain-Shams University Hospitals

Cairo, Egypt

Actively Recruiting

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Research Team

I

Ibrahim Mamdouh Esmat

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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