MedPath

Quality and Outcome Measurements of Urological Patients

Recruiting
Conditions
Urologic Diseases
Registration Number
NCT04763538
Lead Sponsor
Insel Gruppe AG, University Hospital Bern
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
2000
Inclusion Criteria
  • All patients treated at the study sites, signed informed consent
Exclusion Criteria
  • No consent to record medical history

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Disease specific primary endpoint4-5 years

Neuronal networks will be trained to define the respective endpoints for the diseases

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Roland Seiler

🇨🇭

Biel, Switzerland

Department of Urology, Hospital Center Biel

🇨🇭

Biel, Switzerland

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