Predictive Factors in Maxillary and Mandibular Nerve Radiofrequency Treatment for Trigeminal Neuralgia
NCT ID: NCT06240494
Last Updated: 2024-03-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
58 participants
OBSERVATIONAL
2022-09-01
2023-12-02
Brief Summary
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Detailed Description
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Pain intensity was evaluated at baseline and 3 months after US-guided maxillary and/or mandibular nerve PRF treatment using NRS (numerical rating scale). The primary outcome measure was percent reduction in pain, with 50% pain relief lasting at least 3 months was defined as a positive categorical outcome.
In addition, demographic data such as age (years), gender, duration of pain (months), etiology (idiopathic or secondary), MRI findings (normal findings or abnormal findings due to conditions such as vascular compression and demyelinating plaque), pain side (unilateral or bilateral), and history of Gasser ganglion RF ablation were obtained from patient data. NRS scores before and 3 months after PRF were collected from the patient data and recorded. Pre-procedural cranial MRI and MR cisternography reports were accessed from patient records, and any abnormalities were recorded. We retrospectively analyzed the patient's electronic medical history records and the archive system containing the imaging results to obtain the variables.
The main aim of this study was to determine the clinical and demographic variables associated with treatment outcomes in patients with TN who underwent PRF of the maxillary and mandibular nerves. The secondary aim of this study was to determine the incidence of procedure-related adverse events.
Conditions
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Study Design
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OTHER
RETROSPECTIVE
Interventions
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Maxillary nerve and mandibular nerve pulsed radiofrequency
For maxillary nerve pulsed radiofrequency, the lineer transducer is placed distal and parallel to the zygomatic arch, bridging the coronoid and condylar processes and a 22 gauge 6 mm RF cannula was inserted into the target area. With sensory stimulation, patients experienced a distinct sensation in upper jaw, teeth, and palate. Then, PRF treatment was performed at 42 °C for 240 seconds.
For mandibular nerve pulsed radiofrequency, the transducer was placed distally and parallel to the zygomatic arch, bridging the coronoid and condylar processes. The pterygopalatine fossa was visualized and the needle was inserted to target area. With sensory stimulation, patients experienced a distinct sensation in the lower jaw and teeth. With motor stimulation, a throwing movement of the jaw was observed with contraction of the masseter and temporal muscles. PRF treatment was performed at 42 °C for 240 s.
Eligibility Criteria
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Inclusion Criteria
* No response to conservative treatment for \> 3 months
* Magnetic resonance imaging within 1 year prior to injection
* Access to clinical data
Exclusion Criteria
* Patients lost to follow-up within three months after the procedure
* History of surgery or gamma-knife radiosurgery for trigeminal neuralgia
* History of malignancy
18 Years
80 Years
ALL
No
Sponsors
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Diskapi Teaching and Research Hospital
OTHER
Responsible Party
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Damla Yürük
Medical doctor
Principal Investigators
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Ömer Taylan Akkaya, MD
Role: PRINCIPAL_INVESTIGATOR
Diskapi Teaching and Research Hospital
Ezgi Can, MD
Role: STUDY_DIRECTOR
Diskapi Teaching and Research Hospital
Locations
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Ankara Etlik City Hospital
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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Maxillary and mandibular RF
Identifier Type: -
Identifier Source: org_study_id
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