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Additional ethical approvals were requested but not required in Germany (Working Group of Medical Ethics Committee), Spain (Ethics Committee at the Hospital Clínic in Barcelona) and Italy (Tuscany Regional Commission of Bioethics).
According to local ethics standards no formal ethical approval was requested.
For this trial a nationwide ethical approval was requested for The Netherlands and local ethical approval was requested for all participating centres by their local ethical committee.
Ethical approval was requested from the Committee for Medical Research Ethics, Lunds University Hospital, Sweden.
No further ethical approval was requested as the primary focus of these sessions is teaching.
As all data were collected as part of medical care, no ethical approval was requested.
For this reason no ethical approval was requested according to the Dutch Medical Research Involving Human Subjects Act (WMO) [ 11].
Since the data reported in our study was collected by patient's chart review, and no additional information or any other intervention was made for the purpose of the study, no specific ethical approval was requested according to the regulations of our institute.
Therefore, ethical approval was not requested from our ethical review board.
Ethical approval will be requested before the start of this part of the study.
As the framework does not involve human participants, ethical approval is not requested.
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