Measuring quality and outcomes in urological patients
Quality and Outcome Measurements of Urological Patients
This study is trying to gather information from patients with urological conditions to see how well different treatments are working and improve care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Insel Gruppe AG, University Hospital Bern Academic / other |
| Locations | 2 sites (Biel and 1 other locations) |
| Trial ID | NCT04763538 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include all patients receiving treatment for urological diseases at the participating sites who provide informed consent.
Not a fit: Patients who do not consent to the recording of their medical history will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of treatment outcomes in urological diseases, leading to improved patient care.
How similar studies have performed: While similar observational studies have been conducted, the use of neural networks for defining clinical endpoints in this specific context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patients treated at the study sites, signed informed consent Exclusion Criteria: * No consent to record medical history
Where this trial is running
Biel and 1 other locations
- Roland Seiler — Biel, Switzerland (Not_yet_recruiting)
- Department of Urology, Hospital Center Biel — Biel, Switzerland (Recruiting)
Study contacts
- Study coordinator: Roland Seiler, Prof.
- Email: Roland.Seiler@insel.ch
- Phone: +41316321349
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.