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Comparative Study of CT and Fluoroscopic Guided Genicular Nerve Ablation in the Treatment of Knee Osteoarthritis

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Study completion date changed from estimate of May 30, 2025 to Dec 30, 2025 Show 6 more changesShow less
    • Trial completed
    • Final enrollment: 80 participants (planned 60)
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 2 of 3 entries
    • Study description expanded, about 12 words
    • Site details revised
  2. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Jan 30, 2025 to Apr 30, 2025
    • Study completion date: Mar 30, 2025 to May 30, 2025
    • Start date changed from estimate of Jul 30, 2024 to Sep 29, 2024
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this study is to evaluate the comparative effectiveness of CT-guided and fluoroscopic-guided genicular nerve ablation in reducing knee pain and improving function in adults diagnosed with knee osteoarthritis refractory to conservative treatment. The main questions it aims to answer are: * Does CT-guided genicular nerve ablation provide superior pain relief compared to fluoroscopic-guided genicular nerve ablation? * Is there a significant difference in functional improvement between the two techniques? Researchers will compare the outcomes between the CT-guided and fluoroscopic-guided groups to determine which method achieves better pain relief, functional enhancement, safety profile, and patient satisfaction. Participants will: * Undergo either CT-guided or fluoroscopic-guided genicular nerve ablation. * Attend scheduled follow-up visits to assess pain levels, knee function, and any adverse events. * Complete standardized questionnaires to provide feedback on pain relief, functional improvement, and overall satisfaction with the procedure.
Trial Details
NCT Number NCT06514703
Lead Sponsor Zagazig University
Conditions
(from sponsor)		 Osteoarthritis, Knee
Related terms Agnosia, Osteoarthritis, Knee, Patient Satisfaction
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov