van Rijswijk, Joukje http://orcid.org/0000-0002-2413-798X
van Welie, Nienke
Dreyer, Kim
van Hooff, Machiel H. A.
de Bruin, Jan Peter
Verhoeve, Harold R.
Mol, Femke
Kleiman-Broeze, Kimiko A.
Traas, Maaike A. F.
Muijsers, Guido J. J. M.
Manger, Arentje P.
Gianotten, Judith
de Koning, Cornelia H.
Koning, Aafke M. H.
Bayram, Neriman
van der Ham, David P.
Vrouenraets, Francisca P. J. M.
Kalafusova, Michaela
van de Laar, Bob I. G.
Kaijser, Jeroen
van Oostwaard, Miriam F.
Meijer, Wouter J.
Broekmans, Frank J. M.
Valkenburg, Olivier
van der Voet, Lucy F.
van Disseldorp, Jeroen
Lambers, Marieke J.
Peters, Henrike E.
Lier, Marit C. I.
Lambalk, Cornelis B.
van Wely, Madelon
Bossuyt, Patrick M. M.
Stoker, Jaap
van der Veen, Fulco
Mol, Ben W. J.
Mijatovic, Velja
Funding for this research was provided by:
ZonMw (837001504)
Article History
Received: 15 January 2018
Accepted: 26 April 2018
First Online: 9 May 2018
Ethics approval and consent to participate
: This study is approved by the National Central Committee on Research involving Human Subjects (CCMO – NL50484.029.14), by the ethics committee of the VU Medical Centre Amsterdam (Ref. No. 2014/454) which suffices for all participating centers under Dutch law and by the boards of all participating hospitals. The trial is registered in the Dutch Trial Register (NTR 4746, ExternalRef removed).Eligible women receive oral and written information during their regular outpatient visit by the attending gynecologist or fertility doctor. Women will be contacted by telephone for further information by the investigator. Women who agree to participate will be asked to sign written informed consent, of which they will receive a copy at their next visit, when the informed consent form will also be signed by the investigator, supervising gynecologist, the attending registrar or fertility doctor.
: VM received a grant from ZonMW (see funding) to execute this trial. IQ Medical Ventures provides the ExEm FOAM® kits. The authors declare that they have no competing interests.
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