Fries, N.
Dhombres, F.
Massoud, M.
Stirnemann, J. J.
Bessis, R.
Haddad, G.
Salomon, L. J.
Article History
Received: 9 November 2020
Accepted: 8 February 2021
First Online: 27 February 2021
Ethics approval and consent to participate
: Ethics approval: This study was carried out as part of routine care and did not change the patient’s management. In accordance with French laws in force at the time the biometric data of the initial study were collected, such a study did not require an IRB approval (Comité de protection des personnes - Hopital de Poissy Saint Germain en Laye 20, rue Armagis 78105 Saint-Germain-en-Laye; Numéro ID RCB: 2014-A00576–41).Ethical guidelines and informed consent statement: All participating sonographers had, after oral explanations, to obtain the women’s oral informed consent to the fully anonymized use of fetal biometric data collected during routine examinations. For the purpose of the current study, only patients with biometric measurements from 18 weeks onwards were used.
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