RecruitingNot applicableEN originalBladder cancer

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.

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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

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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