54
Participants
Start Date
March 30, 2024
Primary Completion Date
January 30, 2026
Study Completion Date
January 30, 2027
5 mL of 0.5% preservative-free bupivacaine
IV will be inserted. Patient will be connected to cardiorespiratory monitors. The neck will be cleansed twice. A high frequency (15-6 MHz) linear ultrasound probe will be used to identify the arteries, jugular vein, and other important vasculature. Once a clear path for the needle is identified, the skin is anesthetized. A cutting tip spinal needle is then inserted at the lateral aspect of the field and advanced in-plane under ultrasound visualization. A test injection is injected to verify placement, then 5 mL of 0.5% preservative-free bupivacaine will be injected. Per standard SGB procedure, vitals will be measured post-SGB and participants will remain in the clinic for approximately 15 minutes to monitor for any serious adverse events.
The Royal Ottawa Mental Health Centre, Ottawa
Collaborators (1)
Ottawa Hospital Research Institute
OTHER
The Royal's Institute of Mental Health Research
OTHER