Registry Register
The goal of a registry is to enroll the highest possible number of patients in order to collect data. Patients who have a common attribute – e.g. are suffering from the same disease or receiving the same certain treatment – can become part of the registry. If the patients agree to participate, they give their consent that demographic data, treatment information, and endpoints or further previously defined data are being collected about them. No intervention will take place. Deutsche Erklärung