The main objective of this post-marketing observational study (PMOS) is to collect data of using general anesthesia in patients undergoing any surgery to create local recommendations. These data will be based on the evaluation of volatile induction and maintenance anesthesia (VIMA) with Sevorane® (sevoflurane) in adult patients requiring general anesthesia for surgery in terms of quality of anesthesia and its influence on the cardiovascular system in common clinical practice in Ukraine.
Age range
18 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Time to Loss of Consciousness of Patients Administered Anesthesia
Timeframe: Up to 16 minutes
Time to Awakening of Patients
Timeframe: Every minute after anesthesia was stopped until the patient responded to a verbal command
Time to Extubation of Patients
Timeframe: Every minute after anesthesia was stopped until extubation occurred
Anesthesiologists' Satisfaction With Using Sevorane for Induction and Maintenance Anesthesia
Timeframe: Day 1
Patients' Overall Impression of the Anesthesia With Sevorane
Timeframe: Day 1