Actively Recruiting
Lumbar Disc Hernia, Erector Spinae Plane Block, Ilesi
Led by Diskapi Teaching and Research Hospital · Updated on 2025-09-25
80
Participants Needed
1
Research Sites
14 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study is designed as an observational study. Patients who have been treated and completed treatment for lumbar discopathy in our clinic will be followed. Patients will not be divided into groups beforehand, and this will not cause changes to the treatment plan. Patients who have undergone fluoroscopy-guided lumbar interlaminar epidural steroid injection (LESI) and ultrasound-guided lumbar erector spinae plane block (LESP), routinely performed in our clinic for the treatment of back and leg pain due to lumbar disc herniation, will be compared to the effectiveness of these methods on pain at baseline before the procedure and at 2, 6, and 12 weeks afterward using the Visual Analogue Scale for Pain Relief (VAS) and Oswestry Disability Index (ODI). The baseline values will be recorded from the patient files and by request before the start of follow-up.
CONDITIONS
Official Title
Lumbar Disc Hernia, Erector Spinae Plane Block, Ilesi
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with chronic low back pain caused by L4-L5 and L5-S1 lumbar disc herniation confirmed by MRI
- Low back pain greater than 5 on the Visual Analog Scale lasting more than 6 weeks
- Pain has not improved sufficiently with conservative treatments like analgesics and physical therapy
You will not qualify if you...
- Previous lumbar spine surgery
- Spinal deformity or stenosis
- Uncontrolled diabetes
- Allergy to study drugs
- Psychiatric conditions
- Local or systemic infection
- Blood clotting disorders
- Rheumatological diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Etlik City Hospital
Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
E
EMINE YUKSEL
CONTACT
G
GOKHAN YILDIZ
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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