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Chronic Unilateral Lumbar Radicular Pain

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06092749
Enrollment
80
Registered
2023-10-23
Start date
2023-11-01
Completion date
2026-07-31
Last updated
2026-06-15

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

Conditions

Neuropathic Pain

Brief summary

Chronic neuropathic lumbar pain is among one of the most widespread complaints of patients.Many approaches have been attempted to target chronic pain, with varying efficacy and risks. Transgrade (TG) epidural injection is a new technique using a Racz- Coudé needle for epidural access at a "transgrade" angle without requiring any specialized hardware or accessories. Interlaminar (IL) epidural steroid injection (ESI) is one of the procedures that involves the delivery of injectate to the epidural space through directing a needle between the laminae of two adjacent vertebrae.

Interventions

OTHERTransgrade technique (TG)

Transgrade (TG) Epidural Steroid Injection technique

OTHERInterlaminar technique (IL)

Interlaminar (IL) Epidural Steroid Injection technique

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \> 6-month history of persistent pain in one leg with back pain. * Capable of giving informed consent. * Unsatisfactory response to conventional treatments including physical therapy or medications with a numeric rating scale (NRS) ≥ 5.

Exclusion criteria

* Previous lumbar spinal surgery. * Myelopathy. * Rheumatoid disorders. * Psychiatric disorders * Bleeding or coagulation disorders

Design outcomes

Primary

MeasureTime frameDescription
Number of patients who experienced successful pain relief at 3 month post-intervention6 month post intervention (study period)Number of patients who experienced successful pain relief at 3 month post-intervention, which is defined as ≥ 50% reduction of numeric rating scale (NRS-11) from pre-intervention level.

Countries

Egypt

Contacts

CONTACTIbrahim Mamdouh Esmat
ibrahim_mamdouh@med.asu.edu.eg01001241928

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 16, 2026