Bank of Biological Material From Patients and Healthy Donors for the Study of Urological and Uro-oncological Pathologies
Creation of a Bank of Biological Material From Patients and Healthy Donors (Biobank) for the Study of Urological and Uro-oncological Pathologies - URBBAN
1 other identifier
observational
15,000
1 country
1
Brief Summary
The project aims to collect fresh biological material derived both from surgical resections performed in diseases, neoplastic and otherwise, of urological relevance at the level of the prostate, bladder, kidney, testicle and genitourinary organs, and from peripheral blood or other fluids biological samples such as urine, seminal fluid, buccal mucosa, feces or saliva, when available.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2010
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 7, 2010
CompletedFirst Submitted
Initial submission to the registry
December 14, 2023
CompletedFirst Posted
Study publicly available on registry
January 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 6, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 6, 2030
January 10, 2024
December 1, 2023
20 years
December 14, 2023
January 8, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Biological sample
A biobank is a facility aimed at the collection, management, preservation and distribution of biomaterials and related data for research purposes
Baseline
Interventions
Biological samples will be collected from the patient at the time of their access to the Hospital
Eligibility Criteria
People with urological or uro-oncological diseases and infertility
You may qualify if:
- Male and female patients with an age \> 18
- Ability to read and sign the informed consent
- patients affected by urological or uro-oncological diseases
You may not qualify if:
- People with an age \< 18
- Incapacity to read and sign the informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
IRCCS Ospedale San Raffaele
Milan, Lombardy, 20132, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof
Study Record Dates
First Submitted
December 14, 2023
First Posted
January 3, 2024
Study Start
October 7, 2010
Primary Completion (Estimated)
October 6, 2030
Study Completion (Estimated)
October 6, 2030
Last Updated
January 10, 2024
Record last verified: 2023-12
Data Sharing
- IPD Sharing
- Will not share