Ezendam, Nicole P. M.
de Rooij, Belle H.
Kruitwagen, Roy F. P. M.
Creutzberg, Carien L.
van Loon, Ingrid
Boll, Dorry
Vos, M. Caroline
van de Poll-Franse, Lonneke V.
Funding for this research was provided by:
KWF Kankerbestrijding (IKZ 2014-6677)
Article History
Received: 6 December 2017
Accepted: 27 March 2018
First Online: 16 April 2018
Ethics approval and consent to participate
: Medical Ethics approval has been obtained by the Brabant Medical Ethics Committee (MEC) before the start of this project (no. 2015.011). A local research declaration has been obtained for each participating hospital. The study will be conducted in full conformation with the ethical principles of the Declaration of Helsinki Seoul, 2008 and Dutch laws. Informed consent will be asked by the treating gynecologist during the postoperative visit. The patient is provided information about the study and an informed consent form. Patients have at least two weeks to consider the proposal. After the patient provides informed consent, the patient completes the informed consent form, which is filed in the hospital.
: Informed consent includes consent for publication.
: The authors declare that they have no competing interests. The study funders did not/ will not have any role in the design of the study; collection, management, analysis, and interpretation of data; writing of manuscripts; and the decision to submit the manuscripts for publication.
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