Bio Clinical Collection of Urothelial Carcinoma
MicroBlad
1 other identifier
observational
1,000
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2021
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
First Submitted
Initial submission to the registry
July 8, 2021
CompletedFirst Posted
Study publicly available on registry
July 21, 2021
CompletedStudy Start
First participant enrolled
November 16, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 14, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 14, 2031
March 19, 2026
March 1, 2026
4.7 years
July 8, 2021
March 16, 2026
Conditions
Keywords
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
Interventions
blood, urines, stool will be collected during routine cares. Tumor samples from surgery will also be stored.
Eligibility Criteria
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
Biospecimen
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
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mathieu Roumiguie, MD, PhD
University Hospital, Toulouse
Central Study Contacts
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