Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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