Comparison of the Radiofrequency Treatments for the Treatment of Trigeminal Neuralgia.
- Conditions
- Trigeminal Neuralgia
- Interventions
- Procedure: radiofrequency of the peripheral trigeminal branchesProcedure: radiofrequency of gasserian ganglion
- Registration Number
- NCT05516888
- Lead Sponsor
- Diskapi Teaching and Research Hospital
- Brief Summary
The aim of this study is to compare the efficacy of radiofrequency of the Gasserian ganglion versus peripheral branches of the trigeminal nerve for the treatment of trigeminal neuralgia.
- Detailed Description
Trigeminal neuralgia (TN) is defined as sudden, severe, short-term, stabbing and recurrent pain in the distribution of one or more branches of the trigeminal nerve. Many invasive treatments are available for patients who respond poorly to medical therapy. Among them, radiofrequency therapy is a viable option with a reliable initial and long-term clinical efficacy.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- Diagnosed with Primary Trigeminal Neuralgia meets the criteria of the International Classification of Headache Disorders.
- Suffering from severe trigeminal neuralgia that cannot be alleviated effectively with conservative therapy.
- Agree to participate in the study
- Infection at the puncture site.
- Coagulation disorder.
- Abnormal blood test (hepatic or renal function)
- History of receiving invasive treatment (glycerol rhizolysis, radiofrequency thermocoagulation, balloon compression, gamma knife treatment, microvascular decompression)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Radiofrequency of peripheral branches of the trigeminal nerve radiofrequency of the peripheral trigeminal branches pulsed radiofrequency treatment of the peripheral branches of the trigeminal nerve Radiofrequency of gasserian ganglion radiofrequency of gasserian ganglion radiofrequency ablation of the gasserian ganglion
- Primary Outcome Measures
Name Time Method The modified Barrow Neurological Institute Pain Intensity Score six months The efficacy of the treatment will be assessed using the modified Barrow Neurological Institute Pain Intensity Score (I: No pain, off medications; II: Occasional pain, off medications; IIIa: No pain, continued use of medications; IIIb: Pain persists, but adequately controlled with medications; IV: Pain not adequately controlled with medications; V: No relief).
- Secondary Outcome Measures
Name Time Method Patient satisfaction six months Patient satisfaction scores on the 5-point Likert scale (1: poor, 2: fair, 3: good, 4: very good, 5: excellent)
Numeric rating scale baseline to six months Pain will evaluated by a numerical rating scale (0 indicates no pain, 10 indicates the most severe pain imaginable).
Trial Locations
- Locations (1)
Diskapi Yildirim Beyazit Training and Research Hospital
🇹🇷Ankara, Turkey