Actively Recruiting
FASt Track in Elective Neurosurgery: the Role of Low Propofol Bis-NOL Guided General Anaesthesia for Full, Early and Safe Awakening
Led by Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta · Updated on 2026-02-11
100
Participants Needed
1
Research Sites
106 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the effect of intraoperative sedation dosage on awakening and recovery of consciousness after elective neurosurgical surgery.
CONDITIONS
Official Title
FASt Track in Elective Neurosurgery: the Role of Low Propofol Bis-NOL Guided General Anaesthesia for Full, Early and Safe Awakening
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with supra- and subtentorial neurosurgical pathology
- Age greater than or equal to 18 years
You will not qualify if you...
- History of psychiatric illness or current use of psychotropic drugs
- Glasgow Coma Score (GCS) less than 15
- Presence of overt cognitive decline or speech disorders
- Patients younger than 18 years of age
- Intraoperative hypothermia (less than 36 degrees Celsius)
- Intraoperative hypotension (mean arterial pressure less than 20% of baseline)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fondazione IRCCS Istituto Neurologico Carlo Besta
Milan, Italy, 20133
Actively Recruiting
Research Team
C
Carla Carozzi, M.D.
CONTACT
M
Marco Gemma, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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