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)

Fondazione IRCCS Istituto Neurologico Carlo Besta

Milan, Italy

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NCT06844838