Clin2
NCT07239687Possibly a fitRecruiting

Comparing two propofol sedation methods for ICU patients on ventilators

Intensive Care Unit SedationSedationTarget Controlled Infusion of Propofol

Treatments studied

Part of Pain clinical trials.

This study compares two computer-controlled methods for delivering propofol sedation to ICU patients on a breathing machine. It aims to determine which method provides safer and more effective sedation for critically ill patients.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
84 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be 18 years old or older
  • Your ASA physical status must be class I through IV (a measure of overall health)
  • You must be a patient in the Anesthesiology and Reanimation ICU at Hacettepe University Hospital
  • Your medical records and lab results must be available for the study
  • You must be hemodynamically stable (steady blood pressure and heart rate)
  • You cannot have any condition that prevents safe use of propofol (like an allergy or certain lipid disorders) or a neurological disease that would interfere with sedation monitoring

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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