Clinical Trial

Sidekick vs Conventional Cannula in Lumbar Medial Branch Radiofrequency Ablation

Study acronym: SIDE-RFA
Completed
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Summary
Lumbar facet joint-mediated chronic low back pain is a common cause of disability. Radiofrequency ablation (RFA) of the lumbar medial branches is an established interventional pain treatment. Different cannula designs may influence lesion geometry and clinical outcomes. This prospective randomized study aims to compare the clinical outcomes of conventional cannulas and sidekick cannulas used during lumbar medial branch radiofrequency ablation. Patients with chronic lumbar facet joint pain who meet inclusion criteria will be randomly assigned to receive RFA using either a conventional cannula or a sidekick cannula technique. The primary objective is to evaluate pain reduction following the procedure. Secondary outcomes include functional improvement and duration of pain relief during follow-up.
Trial Details
NCT Number NCT07475689
Lead Sponsor Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Conditions Facet Joint Pain; Low Back Pain
Enrollment 82 participants
Start Date 2024-08-01
Primary Completion 2025-08-01 (estimated)
Study Completion 2025-09-24 (estimated)
Updated on ClinicalTrials.gov 2026-03-16