Measuring quality and outcomes in urological patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to collect and analyze various parameters from urological patients treated at specific sites. Data will be stored in multilayered databases, and once a sufficient sample size is reached, neural networks will be utilized to identify clinical endpoints. The study will include patients with uro-oncological conditions as well as other urological diseases, focusing on standard care practices.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All patients treated at the study sites, signed informed consent

Exclusion Criteria:

* No consent to record medical history

Where it's running

• Department of Urology, Hospital Center Biel
  Biel, Switzerland Recruiting
• Roland Seiler
  Biel, Switzerland Not yet recruiting

Study contacts

• Study coordinator: Roland Seiler, Prof.
• Email: Roland.Seiler@insel.ch
• Phone: +41316321349

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.