RecruitingNCT06844838
FASt Track in Elective Neurosurgery: the Role of Low Propofol Bis-NOL Guided General Anaesthesia for Full, Early and Safe Awakening
Sponsor
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Enrollment
100 participants
Start Date
Jan 19, 2024
Study Type
OBSERVATIONAL
Conditions
Summary
To evaluate the effect of intraoperative sedation dosage on awakening and recovery of consciousness after elective neurosurgical surgery.
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is testing whether using a lower dose of a sedative called propofol — guided by two real-time monitors that track brain activity and pain response during surgery — allows brain surgery patients to wake up earlier and more safely after their operation.
**You may be eligible if...**
- You are 18 or older
- You are scheduled for elective (non-emergency) brain surgery for a condition above or below the brain's "tent" (supra- or sub-tentorial)
- You are otherwise in good cognitive and physical health before surgery
**You may NOT be eligible if...**
- You have a history of psychiatric illness or take psychiatric medications
- Your score on the Glasgow Coma Scale is below 15 (meaning you have some impairment before surgery)
- You have obvious cognitive decline or speech difficulties
- You are under 18 years old
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06844838