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The study complied with the MR001 reference methodology with regard to the French Data Protection Authority (CNIL). Informed consent was obtained from all individual participants included in the study. The trial protocol was reviewed and approved by a French National IRB (CPP Nord-Ouest I). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and\/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics Approval and Consent to Participate"}},{"value":"The authors declare no competing interests.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of Interest"}}]}}