Study to Assess the Impact of the Urine Test Cxbladder Triage Plus on the Number of Cystoscopies Performed on Patients With Invisible Blood in Their Urine.
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
This study includes adult patients who see a urologist because of blood in their urine. The amount is so small it can only be seen with a microscope. This is called microhematuria. There can be many reasons for microhematuria. One of them is bladder cancer. While bladder cancer is one of the biggest worries, it is only found in few of these patients. Most microhematuria patients will have a cystoscopy to look inside the bladder. During a cystoscopy, a small camera is inserted into the bladder. This is done through the urethra, the tube that passes urine from the bladder to the outside. In some patients it can cause pain or anxiety. Not all patients have a cystoscopy. Those that don't, usually return for a urine sample within 6 months. This is done to check if there is still blood in their urine. This study is conducted to find out if the use of "Cxbladder Triage Plus" changes the number of cystoscopies in microhematuria patients. Cxbladder Triage Plus is also called "Triage Plus". It is a lab test that was developed to check how likely urothelial carcinoma is present in the bladder. Urothelial carcinoma is by far the most common type of bladder cancer. For the test, the patient voids some urine into a cup. A laboratory then checks the urine of specific genetic material. Abnormalities can be a sign of urothelial carcinoma. The result indicates if the urine is more like most normal urine or more like that of urothelial carcinoma patients. The study is done to find out how Triage Plus changes the number of cystoscopies. Study participants first void urine into a cup. The urine is used for the Triage Plus test. The patients are then assigned to one of two groups. The assignment is random. This means the nobody can influence the assignment. The chance to be assigned to either group is the same. In the test group, the urologist will receive the Triage Plus result and discuss it with the patient. Together they decide whether to do a cystoscopy. In the control group, the urologist will not receive the Triage Plus result. The patient will also not get the result. The urologist and patient will follow standard of care to decide whether to do a cystoscopy. For test group patients, the study gives a recommendation whether to proceed with cystoscopy. It is based on the patient's Triage Plus result. The urologist and patient do not need to follow the recommendation. If the urologist does not follow it, they will complete a survey. The survey has only one question. It is asking for the reasons of the decision. After making their decision, patients will follow the chosen pathway. Data on the performed procedures are collected. The diagnosis will also be documented. Data will be collected for up to about 9 months. To see how Triage Plus changes the number of cystoscopies, these will be counted in each group and then compared.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Pacjent ma skierowanie do urologa z powodu niedawnego krwawienia z dróg moczowych, widocznego tylko pod mikroskopem lub potwierdzonego testem paskowym.
- •Pacjent potrafi oddać próbkę moczu.
- •Pacjent jest w stanie zrozumieć i podpisać zgodę na udział w badaniu.
- •Pacjent zgadza się przestrzegać wymagań badania.
- •Pacjent ma od 19 do 88 lat.
- •Pacjent dobrze rozumie język angielski lub hiszpański (z dostępem do tłumacza).
✗ Disqualifies
- •Pacjent miał wcześniej raka pęcherza lub innych części dróg moczowych.
- •Pacjent miał silne krwawienie z dróg moczowych wymagające hospitalizacji w ciągu ostatniego roku.
- •Pacjent przeszedł operację rekonstrukcji pęcherza.
- •Istnieją inne wskazania do wykonania badania pęcherza, niezwiązane z krwią w moczu.
- •Pacjent miał w przeszłości naświetlania miednicy.
- •Pacjent jest obecnie leczony chemioterapią systemową lub był leczony w ciągu ostatnich 6 tygodni.
- •Pacjent chorował na schistosomatozę.
- •Pacjentka jest w ciąży.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 88 Years
- Last updated (source)
- July 2, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (20)
Urology Centers of Alabama
Homewood, United States
Urology Associates of Mobile
Mobile, United States
Urology Associates of Central California
Fresno, United States
Urology Group of Southern California
Los Angeles, United States
Comprehensive Urology
Los Angeles, United States
Advanced Urology Institute - Daytona Beach
Daytona Beach, United States
Urologic Specialists of Northwest Indiana
Merrillville, United States
Southern Urology
Lafayette, United States
Chesapeake Urology Research Associates
Hanover, United States
Summit Health
Voorhees Township, United States
Albany MED Health System
Albany, United States
Integrated Medical Professionals
New York, United States
Premier Medical Group of the Hudson Valley, P. C.
Poughkeepsie, United States
Dayton Physicians Network
Dayton, United States
Penn State Medical Center, Urology Research
Hershey, United States
Urology Associates, P. C.
Nashville, United States
Vanderbilt University Medical Center
Nashville, United States
Austin Urology Institute
Austin, United States
UT Southwestern Medical Center
Dallas, United States
University of Wisconsin-Madison
Madison, United States
Trial contact
Donna Smith
Tony Lough, PhD
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/3/2026.
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