Blet, Alice
,
de Roquetaillade, Charles
Hartmann, Oliver
Struck, Joachim
Mebazaa, Alexandre
Chousterman, Benjamin Glenn
Funding for this research was provided by:
H2020 European Research Council (666328)
Article History
Received: 14 January 2020
Accepted: 17 February 2020
First Online: 28 February 2020
Ethics approval and consent to participate
: The present study was conducted in France, Belgium, The Netherlands, Italy, and Germany. The study protocol was approved by the local ethics committees, and the study was conducted in accordance with Directive 2001/20/EC as well as good clinical practice (International Conference on Harmonization Harmonized Tripartite Guideline version 4 of May 1, 1996, and decision of November 24, 2006) and the Declaration of Helsinki. Patients were included from June 2015 to May 2016.
: Not applicable.
: AM has received speaker’s honoraria from Novartis, Orion, and Servier and fees as a member of the advisory board and/or steering committee from Cardiorentis, Adrenomed, sphingotec, Sanofi, Roche, Abbott, and Bristol-Myers Squibb. EG has received consulting fees from Adrenomed, Roche Diagnostics, and Magnisense and lecture fees from Edwards Lifesciences. OH and JS are employees of sphingotec GmbH, the company that developed and holds patent rights in the bio-ADM assay. BC received fees as a member of an advisory board from Roche Diagnostics. The other authors declare that there are no competing interests.