In clinical research as well as in routine medical care there are just as many risks as in activities of everyday life.

When thinking about participating in the trial, please consider the following aspects: Which damages result from trial participation (e.g. adverse reactions)? How likely are such damages? What are the advantages of the trial treatment?

The specific risks connected to the medical trial treatment are described in the patient informed consent form in great detail and are also explained during a discussion prior to participation.