Status:
RECRUITING
A Comparative Study of Eleveld and Schnider Pharmacokinetic Models for Target-Controlled Infusion of Propofol in Sedation of Mechanically Ventilated ICU Patients
Lead Sponsor:
Hacettepe University
Conditions:
Intensive Care Unit Sedation
Sedation
Eligibility:
All Genders
18+ years
Brief Summary
This prospective observational study aims to compare the clinical performance of two target-controlled infusion (TCI) models, Eleveld and Schnider, for propofol sedation in mechanically ventilated int...
Eligibility Criteria
Inclusion Criteria:
Age over 18 years,
Classified as ASA (American Society of Anesthesiologists physical status) class I-IV,
Being monitored in the Anesthesiology and Reanimation Intensive Care Unit of Hacettepe University Faculty of Medicine Hospital,
Availability of necessary data (medical history, laboratory results, etc.) for analysis,
Hemodynamic stability -
Exclusion Criteria:Patients who refused to participate in the study or did not provide legal consent,
Patients with an ASA (American Society of Anesthesiologists physical status) classification greater than IV,
Transition to an alternative sedation method during the study,
Contraindication to propofol infusion (e.g., propofol anaphylaxis, lipid metabolism disorders),
Patients whose sedation level could not be clinically assessed due to neurological or neurodegenerative diseases,
Patients expected to require sedation for more than 72 hours (to reduce the risk of propofol infusion syndrome)
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Key Trial Info
Start Date :
February 1 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2026
Estimated Enrollment :
84 Patients enrolled
Trial Details
Trial ID
NCT07239687
Start Date
February 1 2025
End Date
January 1 2026
Last Update
November 20 2025
Active Locations (1)
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1
Hacettepe University
Ankara, Turkey (Türkiye)