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Quality and Outcome Measurements of Urological Patients

NCT04763538 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2023-03-10

No results posted yet for this study

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.

Conditions

  • Urologic Diseases

Interventions

OTHER

Standard of care

Patients are treated according to the standard of care for each individual disease.

Sponsors & Collaborators

  • Hospital Centre Biel/Bienne

    collaborator OTHER

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Roland Seiler, Prof. · Department of Urology, University Hospital Bern

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2026-04-30
Completion
2028-04-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04763538 on ClinicalTrials.gov