Sustainable Anaesthesia Practices in EUROPE - a Prospective International Cohort Study (NCT07252973) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Sustainable Anaesthesia Practices in EUROPE - a Prospective International Cohort Study
2,000 participantsStarted 2026-03-01
Plain-language summary
In response to the climate crises, Societies of Anaesthesiology around the globe call for action to reduce the carbon footprint of daily clinical work. They recommend the use of regional and total intravenous anaesthesia, and for inhalational anaesthesia cases, the use of sevoflurane with low fresh gas flow (FGF \< 0.5 lpm) settings. Surprisingly, the type of anaesthesia and ventilation settings commonly used remain largely unknown. This pragmatic observational cross-sectional assessment at all anaesthesia workstations in participating European hospitals in daily routine aims to evaluate anaesthesia practices in the paediatric and adult patient population.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* All patients receiving any form of anaesthesia care-whether general or regional anaesthesia, monitored sedation, or monitoring only-from an anaesthetist at an anaesthesia workstation in participating European hospitals during the selected data-collection recruitment period
Exclusion Criteria:
* Patients (or legal guardians) who decline consent and patients for whom valid informed consent cannot be obtained due to language barriers or other factors preventing adequate information and understanding.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
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.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Type of anaesthesia (inhalational and intravenous general anaesthesia, regional anaesthesia, sedation, combinations, monitoring only)