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Study identifier: NCT06949436 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Ultra-Early Gamma Knife Stereotactic Radiosurgery for TN

Condition: Trigeminal Neuralgia (TN)  ·  Sponsor: University of Alberta

PhasePhase 2
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate Gamma Knife stereotactic radiosurgery (GK-SRS) as an ultra-early treatment option for trigeminal neuralgia (TN). The main questions it aims to answer are: 1. will earlier GK-SRS provide more durable pain relief compared to later GK-SRS? 2. will earlier GK-SRS reduce or eliminate the need for high-dose medical therapy? 3. will earlier GK-SRS have a lower risk of serious complications compared to other first-line treatments? If participants are assigned to GK-SRS treatment group, they will be asked to: • Undergo a preoperative MRI, measurements of heart rate and blood pressure, stereotactic head-frame placement, post-operative management and observation. Both groups will be asked to: * Complete medical histories and neurological examinations. These are part of standard of care. * Participants will be asked a series of questions related to overall physical health, pain severity, and mood. Completing these questionnaires is part of the research activity. It will take approximately 15- 30 minutes to complete. These questionnaires include: The Barrow Neurological Institute Pain Intensity Score, Brief Pain Inventory-Facial (BPI-Facial), Visual Analog Scale (VAS), Medication Quantification Scale (MQS), Hospital Anxiety and Depression Scale (HADS), Pain Catastrophizing Scale (PCS), and the Short Form Health Survey.

This description comes directly from the study's public registry record.

Talk to the study team

Amanda R Lussoso, BA  ·  lussoso@ualberta.ca

Always discuss trial participation with your own doctor first.

Locations (2)

University of Alberta HospitalEdmonton, Alberta, CanadaRecruiting
University of Alberta HospitalEdmonton, Alberta, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06949436