Prediction of Propofol Effect Compartment Concentrations (Propo2022)

Karl Landsteiner University of Health Sciences

Status: Enrolling

Conditions: Analysis of Anaesthesia Depth

Study type: Observational

Funder types: Other

Identifiers

NCT05940142

SF44

Details and patient eligibility

About

The goal of this observational study is to learn about the prediction of the effect of Propofol by means of EEGs. The main questions it aims to answer are:

• Develop models that can reliably predict the effect of Propofol
• Select the most well suited model for clinical practice
• Compare this model to already existing models (e.g. Schnider-model)

Participants will asked to allow us to collect and use the EEG data recorded during the operations.

Enrollment: 150 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age of 18 or older at the time of the signature of the informed consent
• Signed informed consents
• Planned TIVA with Propofol

Exclusion criteria

• Use of extracorporal circulation (e.g., HLM, ECMO)
• Admission to an ICU/IMCU before the operation or planned admission to an ICU/IMCU after the operation
• Administration of Propofol seven days prior to the planned operation
• Missing informed consent
• All contraindications against TIVA (e.g., allergy against Propofol or soy)
• All operations where BIS monitoring cannot be used (e.g., skin lesions on the front)
• Patients for which the administration of Propofol could be potentially harmfull (e.g., severe heart failure with the risk of drop of blood pressure)
• Neurosurgical operations