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Clinical Trials/NCT06187870
NCT06187870
Recruiting
Not Applicable

Creation of a Bank of Biological Material From Patients and Healthy Donors (Biobank) for the Study of Urological and Uro-oncological Pathologies - URBBAN

IRCCS San Raffaele1 site in 1 country15,000 target enrollmentOctober 7, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Urologic Diseases
Sponsor
IRCCS San Raffaele
Enrollment
15000
Locations
1
Primary Endpoint
Biological sample
Status
Recruiting
Last Updated
2 years ago

Overview

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.

Detailed Description

Significant studies have shown the great potential of research based on access to biobanks which has made it possible to conduct studies and obtain important results through retrospective studies carried out on samples collected some time ago. Thanks to the possibility of accessing human biological samples collected and stored in biological banks, great results have been achieved in the medical field. The project aims to collect fresh biological material deriving from surgical resections performed in neoplastic and non-neoplastic pathologies of urological relevance at the level of the prostate, bladder, kidney, testicle and genitourinary organs, both from biological samples of peripheral blood or other fluids such as urine, seminal fluid, buccal mucosa, feces or saliva, when available. The possibility of obtaining biological samples from the patient at the time of the first visit or the first biopsy and, subsequently, in conjunction with a possible surgical intervention, could ideally give the possibility of studying the disease from its possible onset to the possible intervention, evaluating the evolution and possible association with circulating diagnostic and prognostic markers. The establishment of this collection of research material will allow access to samples of extreme value for the pathophysiological study of the disease, its origin, mechanisms and markers of progression. The data obtained can also be correlated with the patient's clinical history in order to build an overall vision potentially useful in the design of new therapeutic strategies.

Registry
clinicaltrials.gov
Start Date
October 7, 2010
End Date
October 6, 2030
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Andrea Salonia

Prof

IRCCS San Raffaele

Eligibility Criteria

Inclusion Criteria

  • Male and female patients with an age \> 18
  • Ability to read and sign the informed consent
  • patients affected by urological or uro-oncological diseases

Exclusion Criteria

  • People with an age \< 18
  • Incapacity to read and sign the informed consent

Outcomes

Primary Outcomes

Biological sample

Time Frame: Baseline

A biobank is a facility aimed at the collection, management, preservation and distribution of biomaterials and related data for research purposes

Study Sites (1)

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