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Authors
Mølstrøm, Simon https://orcid.org/0000-0002-2778-8075
Nielsen, Troels Halfeld
Nordstrøm, Carl-Henrik
Forsse, Axel
Møller, Søren
Venø, Søren
Mamaev, Dmitry
Tencer, Tomas
Theódórsdóttir, Ásta
Krøigård, Thomas
Møller, Jacob
Hassager, Christian
Kjærgaard, Jesper
Schmidt, Henrik
Toft, Palle
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Article History
Received: 16 December 2022
Accepted: 20 February 2023
First Online: 24 February 2023
Declarations
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: The Danish Regional Committee on Health and Research Ethics approved the protocol (MICA-S-20150173 HLP, 01/01/2017). Danish legislation permits immediate inclusion of patients who are unable to provide consent in nonpharmaceutical trials and mandates that consent should be obtained at the first given opportunity after inclusion in the trial. Consent for the inclusion of comatose patients was obtained from a legal representative and a physician with expertise in the clinical area but no affiliation with the trial. A physician obtained proxy consent at the earliest possible opportunity. Informed consent from the patient was obtained if the patient regained consciousness.
: Not applicable.
: None of the authors has any conflict of interest to declare.
