Observational study on the quality of life of outpatients with urologic diseases
Observational Study on the Quality of Life of Patients Attending General Urology, Sexual Medicine, Reproductive Medicine, Uro-oncology, Neuro-urology, Functional Urology Clinics
This study looks at how urologic diseases affect the quality of life for outpatients to see how their treatment and overall health can be improved.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | IRCCS San Raffaele Academic / other |
| Locations | 1 site (Milan, Lombardy) |
| Trial ID | NCT06193850 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the quality of life of patients attending various urology-related clinics, including those focused on sexual medicine, reproductive medicine, and uro-oncology. Data will be collected on clinical conditions, psychological factors, and quality of life metrics, which will be stored in a specially designed database for statistical analysis. The study emphasizes the importance of outpatient management in improving patient outcomes and understanding the impact of urological conditions on overall health. By following patients over time, the study seeks to provide insights into the effectiveness of treatments and the overall patient experience.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are receiving care in urology, sexual medicine, reproductive medicine, functional urology, neuro-urology, or uro-oncology clinics.
Not a fit: Patients under 18 years old or those with mental or physical disabilities that hinder their ability to complete questionnaires may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies and enhanced quality of life for patients with urologic diseases.
How similar studies have performed: Previous studies have shown that outpatient management significantly impacts both the underlying urological conditions and the quality of life of patients, indicating a positive precedent for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * subjects belonging to general urology, sexual medicine, reproductive medicine, functional urology, neuro-urology and uro-oncology clinics. * subjects \>= 18 years old * signature of informed consent Exclusion Criteria: * \- subjects \< 18 years * presence of mental or physical disability that may prevent the patient from answering the questionnaires.
Where this trial is running
Milan, Lombardy
- IRCCS Ospedale San Raffaele — Milan, Lombardy, Italy (Recruiting)
Study contacts
- Principal investigator: Andrea Salonia, MD — IRCCS Ospedale San Raffaele
- Study coordinator: Andrea Salonia, MD
- Email: salonia.andrea@hsr.it
- Phone: 02 2643 5661
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.