Yale University
This prospective observational cohort study will evaluate clinical outcomes and health care resource utilization among adults who, independent of research participation, are clinically scheduled to undergo temporary 60-day occipital nerve peripheral nerve stimulation (PNS) as part of routine care for refractory headache disorders.
The main purpose of this prospective observational cohort study is to evaluate clinical outcomes and health care resource utilization among adults who, independent of research participation, are clinically scheduled to undergo temporary 60-day occipital nerve peripheral nerve stimulation (PNS) as part of routine care for refractory headache disorders. The study will assess changes in headache impact, pain intensity, neck-related disability, patient global impression of change, medication utilization, and headache-related health care utilization over 12 months. The anticipated impact of this r…
Inclusion Criteria: * Diagnosis of a headache disorder for which the treating clinician has independently made the clinical decision to proceed with temporary 60-day occipital nerve PNS as part of routine care, including: * Occipital neuralgia * Chronic migraine * Chronic tension-type headache * Chronic cluster headache * Cervicogenic headache * Clinically scheduled to undergo temporary 60-day occipital PNS as part of routine care. * Ability to provide informed consent. Exclusion Criteria: * Inability to provide informed consent. * Coagulopathy that would prohibit PNS placement. * Severe ps…
Temporary 60-day occipital nerve PNS as part of routine care.
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