Stopped: PI closed the study before any enrollment
The purpose of this study is to evaluate the safety and efficacy of intra-arterial (IA) delivery of Dexamethasone and Ketorolac into the arteries supplying the sphenopalatine ganglion (SPG) - a collection of neurons that plays an important role in headache disorders - in patients with refractory migraine, cluster headache and trigeminal neuralgia. All patients must fail standard treatments prior to enrollment in the trial.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Procedure-Related Adverse Events
Timeframe: up to 1 hour post-procedure
Number of Procedure-Related Adverse Events
Timeframe: 5 hours post procedure
Number of Procedure-Related Adverse Events
Timeframe: 2 weeks post procedure