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Completed NCT07350109

Investigation of Sedation Depth Via BIS Monitoring in ICU After Cardiac Surgery

Conditions: Sedation After Cardiac Surgery

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 50
Sponsor: Medical University of Graz

Location: Medical University Graz Graz Styria

Summary

This study is a non-interventional, observational research project focused on monitoring sedation levels in patients who have undergone cardiac surgery. It uses a tool called Bispectral Index (BIS), which measures brain activity to assess sedation depth. The goal is to understand how often patients experience deep sedation (BIS \

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 years. * Undergoing cardiac surgery with subsequent admission to the ICU * expected duration of invasive mechanical ventilation \> 6 hours postop. * Written informed consent obtained from the patient or legal representative (if the patient is not capable of consent). Exclusion Criteria: * Pre-existing neurological disorders affecting consciousness or sedation assessment (e.g., severe dementia, epileptic encephalopathy). * Acute neurological events in the perioperative period (e.g., stroke, intracranial hemorrhage). * Severe hepatic dysfunction (Child-Pugh Class C). * Participation in another interventional study potentially affecting sedation or cognitive outcomes. * Pregnancy or lactation. * Patients in whom short-term survival is deemed unlikely due to clinical course

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07350109). StuddyBuddy aggregates publicly available trial information.