NCT06187870

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15,000

participants targeted

Target at P75+ for all trials

Timeline
53mo left

Started Oct 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress78%
Oct 2010Oct 2030

Study Start

First participant enrolled

October 7, 2010

Completed
13.2 years until next milestone

First Submitted

Initial submission to the registry

December 14, 2023

Completed
20 days until next milestone

First Posted

Study publicly available on registry

January 3, 2024

Completed
6.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 6, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 6, 2030

Last Updated

January 10, 2024

Status Verified

December 1, 2023

Enrollment Period

20 years

First QC Date

December 14, 2023

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Urologic DiseasesUrologic NeoplasmsInfertility

Condition Hierarchy (Ancestors)

Female Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesUrogenital NeoplasmsNeoplasms by SiteNeoplasmsGenital Diseases

Central Study Contacts

Anna Maria Ferrara

CONTACT

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

Locations