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Authors
Knol, Ronny http://orcid.org/0000-0003-2436-3343
Brouwer, Emma
van den Akker, Thomas
DeKoninck, Philip L. J.
Lopriore, Enrico
Onland, Wes
Vermeulen, Marijn J.
van den Akker–van Marle, M. Elske
van Bodegom–Vos, Leti
de Boode, Willem P.
van Kaam, Anton H.
Reiss, Irwin K. M.
Polglase, Graeme R.
Hutten, G. Jeroen
Prins, Sandra A.
Mulder, Estelle E. M.
Hulzebos, Christian V.
van Sambeeck, Sam J.
van der Putten, Mayke E.
Zonnenberg, Inge A.
Hooper, Stuart B.
te Pas, Arjan B.
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Funding
Funding for this research was provided by:
ZonMw (852001902)
Gisela Thier Fund
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Article History
Received: 1 August 2022
Accepted: 26 September 2022
First Online: 1 October 2022
Declarations
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: The study is and will be conducted according to the principles of the Declaration of Helsinki and in accordance with the Dutch law (Medical Research Involving Human Subjects Act). The study protocol (study ID number NL67770.058.18) is evaluated and approved by the MREC of the LUMC (reference P18.218). Parental consent is required before trial participation.
: Not applicable.
: The authors declare that they have no competing interests. The Concords used in this trial were either designed and built by LUMC (for 3 participating centres) or purchased from Concord Neonatal B.V. (Leiden, The Netherlands; for 6 participating centres). ABtP, SBH and AHvK are members of the Scientific Advisory Board of Concord Neonatal B.V., but have no financial relationship or support. The company has no role in the design of the study; in the collection, analysis or interpretation of the data; or in the writing of the manuscript.
