Staff information Members of the staff at the participating centres will recieve written and oral information concerning the trial. Consent Form Every participant need to fill in the Consent form prior to randomisation Criterias Who can be included in the trial? Doctors What should I be aware of? For the midwife Tasks of the midwife Manuscript How to informe about the trial? Randomisation How to randomise? Download (PDF) Project protocol Flowchart for the staff De-blinding Declaration of participation (Danish) Information for non-participants (Danish) Login Only for trial affiliated staff Randomisation Database Contact Responsible for the trial, Sidsel Boie, MD PhD student Randers Regional HospitalØstervangsvej 288930 Randers NØ Phone number: +45 60 63 68 35 Send a message »
