Clinical Trials in Italy / NCT06844838
Recruiting
Observational
FASt Track in Elective Neurosurgery: the Role of Low Propofol Bis-NOL Guided General Anaesthesia for Full, Early and Safe Awakening
NCT06844838 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Supratentorial Brain Tumor Surgery
Study summary
To evaluate the effect of intraoperative sedation dosage on awakening and recovery of consciousness after elective neurosurgical surgery.
Eligibility
Inclusion Criteria:
* Patients with supra- and sub tentorial neurosurgical pathology who meet the following inclusion criteria will be enrolled:
* Age greater than or equal to 18 years
Exclusion Criteria:
* Psychiatric illness in history and/or taking psychotropic drugs
* Glasgow Coma Score (GCS) \< 15
* Presence of overt cognitive decline or speech disorders
* Patients younger than 18 years of age
* Intraoperative hypothermia (\< 36°)
* Intraoperative hypotension (MAP \< 20% of baseline)
Primary outcome measure(s)
- General Anaesthesia effect on Awakening — 2 years
Correlation between intraoperative dosage of Propofol and Remifentanil with respect to dichotomous outcome related to quality of awakening post GA.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Fondazione IRCCS Istituto Neurologico Carlo Besta | Milan | Italy | Recruiting |
More Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta trials in Italy
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06844838 on ClinicalTrials.gov ↗ ← All trials in Italy