Randomized Study of Cranial Blocks for Postoperative Anesthesia to Reduce Pain and Postoperative Opioid Usage

Randomized Study of Cranial Blocks for Postoperative Anesthesia to Reduce Pain and Postoperative Opioid Usage

Randomized Study of Cranial Blocks for Postoperative Anesthesia to Reduce Pain and Postoperative Opioid Usage

Enrolling By Invitation
18-99 years
All
Phase N/A
  • Simplified description (AI rewritten)
  • Technical description (Original)
If you agree to join the study, on the morning of your procedure, you will be randomized into one of the 3 study groups by the research team. 

After your procedure, you will have your blood taken for 3 days to monitor for a potential drug interaction. You will then be asked to complete pain surveys while in the hospital. Participation in this clinical trial will not impact your clinical care and if you need standard of care pain medication, oral or intravenous, to control your pain after surgery, the clinical team will give it to you.

Your participation will last for the duration of your time in the hospital (until discharge). You will have an end-of-study visit at your follow-up appointment 4-6 weeks after your surgery.
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Study details
    craniotomy

N/A

19 February 2024

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