Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06187870

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

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

Long-term Monitoring

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

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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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