Steps to follow:

  1. Check the in- and exclusion criteria (download the inclusion checklist here)

  2. Acquire written informed consent from the patient
  3. Include and randomized the patient through ALEA, the treatment-arm is displayed directly.
  4. Make a note of the study number and assigned treatment in the patient dossier

Please contact the trial coordinator (010-7034519 of 06-17616440) if you encounter any trouble with inclusion.