NCT04970472

Brief Summary

The goal of this study is to collect tumor samples, urines, stool and blood from patients with urothelial carcinoma. These samples will be stored in a secure and confidential laboratory of the Toulouse University Hospital.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
64mo left

Started Nov 2021

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 Progress46%
Nov 2021Jul 2031

First Submitted

Initial submission to the registry

July 8, 2021

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 21, 2021

Completed
4 months until next milestone

Study Start

First participant enrolled

November 16, 2021

Completed
4.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 14, 2026

Expected
5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 14, 2031

Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

4.7 years

First QC Date

July 8, 2021

Last Update Submit

March 16, 2026

Conditions

Keywords

Urothelial Carcinomaneoplasmbladder cancer

Outcome Measures

Primary Outcomes (2)

  • Collection and long-term collection of blood, urines, stool and tumor samples from patients with Urothelial bladder carcinoma for future biological and/or surrogate marker studies.

    Transcriptomic analysis

    Day 0

  • Collection and long-term collection of blood, urines, stool and tumor samples from patients with Urothelial bladder carcinoma for future biological and/or surrogate marker studies.

    Transcriptomic, proteomic and epigenetic analysis

    during the intervention/procedure/surgery

Study Arms (1)

patients with Urothelial bladder carcinoma

collection of blood, urines, stool and tumor samples

Biological: collection of blood, urines, stool and tumor samples

Interventions

blood, urines, stool will be collected during routine cares. Tumor samples from surgery will also be stored.

patients with Urothelial bladder carcinoma

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients will be all enrolled at Toulouse University Hospital during primary cares.

You may qualify if:

  • Adult \>18 years old
  • Patient with suspected or diagnosed Urothelial carcinoma
  • Patients who are willing to consent for this protocol.

You may not qualify if:

  • Pregnant or breastfeeding patients
  • Patients under 18 years old
  • Patients under guardianship or curators
  • Patients unable to sign a free and informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rangueil University Hospital

Toulouse, 31059, France

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Urine, stool, blood and saliva samples will be stored. Tumor samples, collected for primary cares using a punch knife, or a small surgery, will be stored.

MeSH Terms

Conditions

Carcinoma, Transitional CellUrinary Bladder NeoplasmsNeoplasms

Interventions

Defecation

Condition Hierarchy (Ancestors)

CarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeUrologic NeoplasmsUrogenital NeoplasmsNeoplasms by SiteFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesUrinary Bladder DiseasesUrologic DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

Digestive System Physiological PhenomenaDigestive System and Oral Physiological Phenomena

Study Officials

  • Mathieu Roumiguie, MD, PhD

    University Hospital, Toulouse

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Mathieu Roumiguie, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 8, 2021

First Posted

July 21, 2021

Study Start

November 16, 2021

Primary Completion (Estimated)

July 14, 2026

Study Completion (Estimated)

July 14, 2031

Last Updated

March 19, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations