Olfactive Detection of Urothelial Carcinoma by Sniffer Dogs
OUAF
1 other identifier
observational
340
1 country
2
Brief Summary
The aim of this study is to estimate the sensitivity of olfactory detection of urothelial carcinomas of the bladder in urine samples by assistance dogs trained in this practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2025
2 active sites
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
June 20, 2025
CompletedFirst Submitted
Initial submission to the registry
December 10, 2025
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
January 12, 2026
December 1, 2025
1.2 years
December 10, 2025
January 5, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Assess the sensitivity of olfactory detection of urothelial carcinomas of the bladder in urine samples by assistance dogs trained for this purpose
Day -60 to Day 0
Study Arms (2)
Positive bladder tumor
Bladder tumor present during cystoscopy and confirmed by pathological examination.
Negative bladder tumor
No bladder tumor on cystoscopy/suspicious lesion but with negative pathological analysis
Interventions
olfactory detection of urothelial carcinoma of the bladder in a urine sample by dogs
Eligibility Criteria
Subject scheduled for any endourological surgery involving an initial cystoscopy, the most common of which are: transurethral resection of the bladder, transurethral resection of the prostate, internal optical urethrotomy, bladder lithoclast, ureteral stent replacement, ureteroscopy, etc. (non-exhaustive list). Recruitment will take place in the urology department, during the preoperative consultation or during hospitalization.
You may qualify if:
- Adult (\> 18 years old)
- Subject scheduled for any endourological surgery involving an initial cystoscopy, the most common of which are: transurethral resection of the bladder, transurethral resection of the prostate, internal optical urethrotomy, bladder lithoclast, ureteral stent replacement, ureteroscopy, etc. (non-exhaustive list)
- Subjects for whom a urine sample (for bacteriological or cytological testing) is planned as part of routine practice in the month prior to the procedure
- Subjects affiliated with a health insurance plan or beneficiaries of such a plan
You may not qualify if:
- Absence of signed informed consent / inability to provide the subject with informed information (emergency situations, difficulties in understanding the subject, etc.)
- Patient under guardianship, conservatorship, or judicial protection
- History of cancer other than urothelial bladder carcinoma, unless in complete remission for \> 5 years
- Pregnant or breastfeeding women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Hôpitaux Civils de Colmar
Colmar, France
Hôpitaux Universitaires de Strasbourg
Strasbourg, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 10, 2025
First Posted
January 12, 2026
Study Start
June 20, 2025
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
January 12, 2026
Record last verified: 2025-12