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Clinical Trials in Turkey / NCT07400068
Starting soon Observational

PLDD With or Without Transforaminal Epidural Steroid Injection in Lumbar Disc Herniation

NCT07400068 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-02-10

Condition(s) studied

Lumbar Disc HerniationLumbar Radiculopathy

Investigational drug(s) / intervention(s)

Percutaneous Laser Disc Decompression (PLDD)Transforaminal Anterior Epidural Steroid Injection

Percutaneous Laser Disc Decompression (PLDD): Routine minimally invasive laser-based disc decompression performed under fluoroscopic guidance to reduce intradiscal pressure in patients with lumbar disc herniation.

Transforaminal Anterior Epidural Steroid Injection: Routine transforaminal anterior epidural injection of dexamethasone performed under fluoroscopic guidance following PLDD during the same session without additional puncture.

Study summary

This prospective observational study aims to evaluate the clinical outcomes of patients with single-level lumbar disc herniation who undergo routine percutaneous laser disc decompression (PLDD).

In routine clinical practice, some patients receive an additional transforaminal anterior epidural steroid injection during the same session without an extra puncture. This study will prospectively follow patients who receive PLDD alone and those who receive PLDD combined with epidural steroid injection.

Pain intensity, functional status, analgesic use, need for additional interventions, and complications will be assessed over time. The results may help to clarify whether adding epidural steroid injection to PLDD improves clinical outcomes in patients with lumbar disc herniation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Age 18 years and older Diagnosis of single-level lumbar disc herniation confirmed by magnetic resonance imaging (MRI) Presence of radicular leg pain refractory to conservative treatment Undergoing routine percutaneous laser disc decompression (PLDD) as part of standard clinical care Ability to provide informed consent Exclusion Criteria: Multilevel lumbar disc herniation Extruded or sequestered disc herniation Severe spinal canal stenosis or spinal instability Previous lumbar spine surgery at the affected level Active infection or systemic inflammatory disease Coagulopathy or use of anticoagulant therapy contraindicating intervention Pregnancy Inability to complete follow-up assessments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mersin University Faculty of Medicine, Department of Algology Mersin Yenişehir

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07400068 on ClinicalTrials.gov ↗ ← All trials in Turkey