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Recruiting Not applicable Interventional

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.

ClinicalTrials.gov ID: NCT06394869

Public ClinicalTrials.gov record NCT06394869. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 5:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Cystoscopic REDuction In BLadder Evaluations for Microhematuria - A Prospective Randomized, Controlled, Clinical Utility Study for Evaluation of Microhematuria (The CREDIBLE Study)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT06394869
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Pacific Edge Limited
Industry
Enrollment
1,000 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
18 Years to 88 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 28, 2025
Primary completion
Sep 30, 2027
Completion
Mar 31, 2028
Last update posted
Jul 1, 2026

2025 – 2028

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Urology Centers of Alabama Homewood Alabama 35209 Recruiting
Urology Associates of Mobile Mobile Alabama 36608 Recruiting
Urology Associates of Central California Fresno California 93720 Recruiting
Urology Group of Southern California Los Angeles California 90017-4007 Recruiting
Comprehensive Urology Los Angeles California 90048 Recruiting
Advanced Urology Institute - Daytona Beach Daytona Beach Florida 32114 Recruiting
Urologic Specialists of Northwest Indiana Merrillville Indiana 46410 Recruiting
Southern Urology Lafayette Louisiana 70508 Terminated
Chesapeake Urology Research Associates Hanover Maryland 21076 Recruiting
Summit Health Voorhees Township New Jersey 08043 Recruiting
Albany MED Health System Albany New York 12208 Recruiting
Integrated Medical Professionals New York New York 11042 Recruiting
Premier Medical Group of the Hudson Valley, P. C. Poughkeepsie New York 12601 Recruiting
Dayton Physicians Network Dayton Ohio 45409 Recruiting
Penn State Medical Center, Urology Research Hershey Pennsylvania 17033 Recruiting
Urology Associates, P. C. Nashville Tennessee 37209 Terminated
Vanderbilt University Medical Center Nashville Tennessee 37232 Recruiting
Austin Urology Institute Austin Texas 78758 Not yet recruiting
UT Southwestern Medical Center Dallas Texas 75390 Recruiting
University of Wisconsin-Madison Madison Wisconsin 53792 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06394869, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 1, 2026 · Synced Sep 5, 2026

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