Freund, Yonathan
Gorlicki, Judith
Cachanado, Marine
Salhi, Sarah
Lemaître, Vanessa
Simon, Tabassome
Mebazaa, Alexandre
Funding for this research was provided by:
Ministère de l’Enseignement Supérieur, de la Recherche Scientifique et des Technologies de l'Information et de la Communication (K170918J)
Article History
Received: 17 December 2018
Accepted: 9 January 2019
First Online: 31 January 2019
Ethics approval and consent to participate
: Informed consent will be obtained from all study participants whenever possible. If the patient is unable to consent, informed consent from a relative will be obtained. If there is no relative, an emergency consent could be obtained. In all cases, the patient’s consent will be obtained as soon as their condition allows it. An Institutional Review Board authorized the study (Comité de Protection des Personnes SOOM 2, ID-RCB: 2018-AO1139–46, 6 September 2018) for all participating centers, as this trial will be conducted in France only.
: Not applicable.
: The authors declare that they have no competing interests.
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