Actively Recruiting
COMparative Performance of General Purpose Models
Led by Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta · Updated on 2026-02-12
42
Participants Needed
2
Research Sites
117 weeks
Total Duration
On this page
Sponsors
F
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Lead Sponsor
U
University Medical Center Groningen
Collaborating Sponsor
AI-Summary
What this Trial Is About
To compare the performance of the Eleveld models for propofol and remifentanil on neurosurgery patients admitted to intensive care with their intraoperative performance.
CONDITIONS
Official Title
COMparative Performance of General Purpose Models
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients undergoing elective neurosurgical procedures with an expected sedation after surgery of > 12 hours
- Requirement for an arterial line
You will not qualify if you...
- Pregnancy
- Known sensitivity or allergy to propofol or remifentanil
- Patient participating in research requiring exclusion due to other study protocols or health authority
- Age under 18 years
- Patients receiving propofol and/or remifentanil infusions not delivered through TCI pumps before inclusion
- Patients exposed to other sedatives (benzodiazepines, volatile anesthetics, quetiapine) before inclusion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Foundation IRCCS Carlo Besta Neurological Institute
Milan, Italy, Italy, 20133
Actively Recruiting
2
Fondazione IRCCS Istituto Neurologico C. Besta
Milan, Milano, Italy, 20133
Actively Recruiting
Research Team
M
Michele Introna, 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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