COMparative Performance of General Purpose Models
ConditionNeurosurgical Patients
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorFondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
About this trial
To compare the performance of the Eleveld models for propofol and remifentanil on neurosurgery patients admitted to intensive care with their intraoperative performance.
Eligibility criteria
Qualifiers
Adult patients undergoing elective neurosurgical procedures with an expected sedation after surgery of > 12 hours • Requirement for an arterial line
Disqualifiers
Pregnancy
Known sensitivity or allergy to propofol or remifentanil
Patient participating in research for which a period of exclusion is currently required by other study protocol, ethical committee or health authority.
Age < 18 years old
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Lead sponsor
University Medical Center Groningen
Collaborator
Source ClinicalTrials.gov