Document is current
Any future updates will be listed below
-
Authors
Willemsen, Sten P.
Knol, Ronny http://orcid.org/0000-0003-2436-3343
Brouwer, Emma
van den Akker, Thomas
DeKoninck, Philip L. J.
Lopriore, Enrico
Onland, Wes
de Boode, Willem P.
van Kaam, Anton H.
Nuytemans, Debbie H.
Reiss, Irwin K. M.
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.
te Pas, Arjan B.
Vermeulen, Marijn J.
-
Funding
Funding for this research was provided by:
ZonMw (852001902)
Stichting Vrienden van het Sophia (S17-14)
- License Information
-
More Information
Article History
Received: 16 May 2023
Accepted: 22 February 2024
First Online: 4 March 2024
Declarations
:
: 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 equipment used in this trial was either designed and built by LUMC (for 3 participating centers) or purchased from Concord Neonatal B.V. (Leiden, The Netherlands; for 6 participating centers). 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 data; or in the writing of the manuscript.
