Stopped: Low enrollment
Single-center, open-label, pre-post treatment pilot study to evaluate the safety and effectiveness of sphenopalatine ganglia blocks for the treatment of chronic migraine in the pediatric population. 50 children with a diagnosis of chronic migraines will undergo a series of three transnasal sphenopalatine ganglia blocks to measure their effect on headache frequency, headache intensity, headache duration, and use of headache medication.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Reduction in frequency of headache days: pre-treatment
Timeframe: Up to 4 weeks following consent
Reduction in frequency of headache days: post-treatment
Timeframe: Up to one year following consent