Actively Recruiting
Creation of a Bank of Biological Material From Patients and Healthy Donors for the Study of Urological and Uro-oncological Diseases
Led by IRCCS San Raffaele · Updated on 2024-01-10
15000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting fresh biological materials from patients and healthy donors to support studies on urological and uro-oncological diseases. This includes samples from surgical removals related to conditions of the prostate, bladder, kidney, testicle, and other genitourinary organs. The study aims to understand disease origins, progression, and links to diagnostic markers by analyzing these samples alongside patients' medical histories. Biological samples such as peripheral blood, urine, seminal fluid, buccal mucosa, feces, and saliva are collected when available, especially during patients' first visits, biopsies, or surgeries. This collection creates a valuable biobank that supports ongoing and future research into urological diseases and cancers. The project is observational and involves gathering and storing these samples for detailed analysis. Participants provide samples at hospital visits, and researchers track baseline biological data to study disease mechanisms and progression. The main focus is on collecting and preserving these samples for research rather than testing treatments. The study accommodates adult male and female participants, including healthy volunteers, and follows participants over time to build a comprehensive resource for understanding urological health conditions.
CONDITIONS
Brief Title
Bank of Biological Material From Patients and Healthy Donors for the Study of Urological and Uro-oncological Pathologies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female patients aged over 18
- Ability to read and sign the informed consent
- Patients affected by urological or uro-oncological diseases
You will not qualify if you...
- People younger than 18 years
- Inability to read and sign the informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to several months depending on participant's clinical care timeline
Participants provide biological samples such as blood, urine, seminal fluid, buccal mucosa, feces, or saliva at the time of their hospital visit or surgical intervention for research purposes.
1 to 2 visits depending on clinical procedures
Duration - Up to several years until study completion
Participants are observed over time to study disease progression and correlate biological samples with clinical history.
Visits as part of routine clinical care; no additional visits required for the study
Trial Site Locations
Total: 1 location
1
IRCCS Ospedale San Raffaele
Milan, Lombardy, Italy, 20132
Actively Recruiting
Research Team
A
Anna Maria Ferrara
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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