About this trial

All patients undergoing urological surgery or treatment should receive standardized questionnaires on quality of life, satisfaction, pain and physical recovery. Indication-specific, individual pathways are set up, for example, for patients with localized prostate cancer, benign prostate enlargement, bladder dysfunction or erectile dysfunction. In combination with the clinical data, the PROM data should help to improve the quality of the results and, if necessary, adapt treatment pathways to patient needs.

Eligibility criteria

Qualifiers

Patients treated at the Department of Urology

≥18 years of age

Active Mail-account, use of smartphone/tablet/PC

Written informed consent

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Observation of patients undergoing sugery

Treatment groups

No treatment groups listed

Locations

1
Röthl Martina Anna8036, GrazStyria, Austria

Sponsors and collaborators

Medical University of Graz

Lead sponsor