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Thank you for participating in our survey that will help to inform about the current practices of ARDS treatment.

It will take you about 20 minutes to complete the survey. No personal data will be collected.

This study was conceived as collaborative project of the University of Hamburg (Department of Intensive Care Medicine, UKE Hamburg-Eppendorf), the University of Trento (Center for Medical Sciences, Santa Chiara Hospital), the University of Genova, and the University of Amsterdam (Department of Intensive Care Medicine, Amsterdam UMC) and is part of the PROtective VEntilation (PROVE) Network.

This survey complies with the General Data Protection Regulation (GDPR) of the European Union to ensure the confidentiality and protection of your data. Participation in this survey is voluntary, and no personal identifiable information will be collected. All responses will be anonymised and used solely for the purposes of this research project to evaluate current practices in the management of ARDS in European ICUs.
By proceeding, you consent to the processing of your responses for research purposes.
 
7% of survey complete.

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