On this page you will find the patient information and consent form, which has been approved by the Danish Ethics Committee. The document can be used as a template, or modified to meet local ethics committee requirements. Please be aware what is necessary in your local ethics committee. In some countries it is not required to get parental consent to look in the health care records of the child, and other places may not even need to ask for new consent for the SafeBoosC-IIIfu, since they have included this in the parental information/consent form at randomisation.
Below you will find a link to the Danish Ethics Review Board approval of the SafeBoosC-III two year follow up study
Danish Ethics Review Board Approval (pdf, will open in a new tab)