Transnasal Sphenopalatine Ganglion Block for Treatment of Acute Subarachnoid Hemorrhage Associated Headache

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18-100
SponsorUniversity of California, Davis

About this trial

The study titled \"Transnasal sphenopalatine ganglion block for treatment of acute subarachnoid hemorrhage associated headache\" is a randomized controlled pilot study aimed at evaluating the efficacy of a transnasal sphenopalatine ganglion (SPG) block in addition to standard pain medication for reducing headache severity in patients with acute subarachnoid hemorrhage (aSAH). The study also examines whether this intervention can reduce opioid requirements during hospitalization and upon discharge.

Eligibility criteria

Qualifiers

Acute subarachnoid hemorrhage

Age greater than 18 years

Secured aneurysm

Patient can verbalize pain score to clinician, nurse, medical translator, or surrogate decision

Disqualifiers

Less than 18 years old

Unsecured aneurysm

Pregnant or lactating

Prisoner

Trial design

Treatments tested in this trial

  • Transnasal sphenopalatine ganglion block

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of California, Davis

Lead sponsor

Agnes Marshall Walker Foundation

Collaborator