Quality and Outcome Measurements of Urological Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInsel Gruppe AG, University Hospital Bern

About this trial

Prospectively, all available parameters of urologic patients treated at the study sites will be acquired and stored in multilayered databases. Upon a given samples size, neuronal networks will be trained to define clinical endpoints. Beside uro-oncological patients also patients with other urological diseases will be enrolled.

Eligibility criteria

Qualifiers

All patients treated at the study sites, signed informed consent

Disqualifiers

No consent to record medical history

Trial design

Treatments tested in this trial

  • Standard of care

Treatment groups

No treatment groups listed

Sponsors and collaborators

Insel Gruppe AG, University Hospital Bern

Lead sponsor

Hospital Centre Biel/Bienne

Collaborator