Heemskerk, S. C. M.
Rotteveel, A. H.
Benninga, M. A.
Baeten, C. I. M.
Masclee, A. A. M.
Melenhorst, J.
van Kuijk, S. M. J.
Dirksen, C. D.
Breukink, S. O.
Funding for this research was provided by:
Ministerie van Volksgezondheid, Welzijn en Sport
Medtronic
Article History
Accepted: 7 February 2018
First Online: 22 February 2018
Compliance with ethical standards
:
: SOB and JM receive an unrestricted grant from Medtronic. The grant provided by Medtronic is partially used for the employment of SCMH. MAB is consultant for Shire, Sucampo, Coloplast, and Norgin.
: The study will be conducted according to the principles of the 1964 Declaration of Helsinki and its later amendments, and in accordance with the Medical Research Involving Human Subjects Act. The study protocol has been approved by the Medical Ethical Committee of the Maastricht University Medical Center/Maastricht University in Maastricht, the Netherlands (METC161044). Written informed consent will be obtained from all participants included in the study, after a screening, and receiving, reading, and discussing the participant information brochure with the researcher. Consent will take place prior to randomization.