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Authors
Lorthe, Elsa
Kayem, Gilles https://orcid.org/0000-0002-8218-8814
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Kayem, Gilles
Lorthe, Elsa
Ancel, Pierre-Yves
Abdoul, Hendy
Briand, Nelly
Lehmann, Blandine
Cabanne, Clémence
Marret, Stéphane
Foix l’Hélias, Laurence
Goffinet, François
Schmitz, Thomas
Charlier, Caroline
Autret, Fanny
Azria, Elie
Balitalike, Jadot
Billiemaz, Kareen
Bohec, Caroline
Bolot, Pascal
Bornes, Marie
Bouchghoul, Hanane
Bourennane, Malek
Bretelle, Florence
Carbillon, Lionel
Castel, Christine
Chauleur, Céline
Corroenne, Romain
Coste, Karen
Datin-Dorrière, Valérie
Desbriere, Raoul
Desfrere, Luc
Dreyfus, Michel
Dommergues, Marc
Durrmeyer, Xavier
Favrais, Géraldine
Flamant, Cyril
Gallot, Denis
Gries, Julie
Haddad, Bassam
Julé, Laure
Laffaille, Cécile
Lepercq, Jacques
Letamendia, Emmanuelle
de Marcillac, Fanny
Miler, Caroline
Morel, Olivier
Norbert, Karine
Perrotin, Franck
Poncelet, Christophe
Renesme, Laurent
Roumegoux, Claire
Rozenberg, Patrick
Ruiz, Mireille
Sentilhes, Loïc
Sibiude, Jeanne
Subtil, Damien
Tillouche, Nadia
Torchin, Héloïse
Tosello, Barthélémy
Verspyck, Eric
Vivanti, Alexandre
Winer, Norbert
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Funding
Funding for this research was provided by:
french ministry of health (PHRCN-16-0212)
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Article History
Received: 30 July 2021
Accepted: 12 August 2021
First Online: 8 September 2021
Declarations
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: Ethics approval was granted by the Committee for the Protection of Persons (CPP) participating in biomedical research Sud Méditerranée IV (Reference 190509, June 11, 2019) and the National Agency for Drug Security (ANSM, Reference EUDRACT 2018–004482-14, August 14, 2019). Women will be included and randomized in the TOCOPROM trial only after receiving adequate information and providing written free and informed consent. The second legal guardian’s consent to neonatal and 2-year and 5-year data collections will be obtained at maternal inclusion or delivery or at 2 years at the latest.
: Not applicable.
: The authors declare that they have no competing interests.
