🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT05889195
Active, not recruiting Observational

Detection and Risk Stratification in Veterans Presenting With Microscopic Hematuria

NCT05889195 · tracked via the Priya Life Science USA tracker
Sponsor
Pacific Edge Limited
Phase
Observational
Started
2023-11-02
Last updated
2026-09-16

Condition(s) studied

Urothelial Carcinoma

Investigational drug(s) / intervention(s)

Cxbladder urine test

Cxbladder urine test: Cxbladder tests uses mRNA and DNA biomarkers in the urine to direct the management of UC from diagnosis to surveillance for disease recurrence.

Study summary

It is currently debated whether the use of invasive standard of care procedures, such as cystoscopy, a procedure which involves inserting a thin camera, called a cystoscope, into the bladder to look for signs of disease, is appropriate for patients with microscopic hematuria (blood in the urine that cannot be seen with the naked eye). This is because the risk of disease (bladder cancer - urothelial carcinoma) is relatively low in this population group, approximately 3%. Invasive procedures such as cystoscopy can cause anxiety and pain, in addition to other potential side effects. This has resulted in low admittance for cystoscopy among patients with hematuria (blood in urine) in urology clinics. Therefore, there is a need for a simpler, non-invasive test that can accurately detect the presence or absence of disease (urothelial carcinoma) in patients with microscopic hematuria. Cxbladder, a non-invasive, urine-based test, has the potential to fill this role.

Eligibility

Sex
ALL
Min age
18 Years
Max age
89 Years
Healthy volunteers
No
Inclusion Criteria: 1. Subjects who are referred to urology and are either scheduled for a cystoscopy or have had a cystoscopic investigation within the last two months for the evaluation of hematuria meeting ONE of the following criteria: EITHER: (a) Microscopic hematuria, confirmed by urine microscopy of three or more RBC/HPF (or equivalent). OR: (b) Gross hematuria. 2. Physically able to provide a voided urine sample from a bladder that has not been surgically altered. 3. Able to give informed, written consent. 4. Able and willing to comply with study requirements (complete at-home urine sampling, fill in test request forms (TRFs) / tube labels and ship urine back to the central laboratory using a prepaid courier service). 5. Aged 18 years or older. Footnotes: 1. For the microscopic hematuria patients, the recruitment priority at each respective site will be: i) Patients who have undergone initial diagnostic cystoscopy and have been scheduled for a later TURBT for suspicious lesion in the bladder. ii) Patients who are considered high risk by the AUA 2020 guidelines. 2. For gross hematuria patients, the recruitment priority at each respective site will be: i) Patients who have undergone initial diagnostic cystoscopy and have been scheduled for a later TURBT for suspicious lesion in the bladder Exclusion Criteria: 1. Prior history of bladder malignancy. 2. Reported Cxbladder results within the last six months. 3. Prior history of upper tract urothelial carcinoma (UC) or prostatic urethral UC. 4. Reconstructed or diverted bladder (e.g., bladder augmentation, ileal conduit, Indiana pouch). 5. Subjects aged 89 years of age or older. 6. Subjects with a history of pelvic radiation. 7. Subjects currently receiving systemic chemotherapy or has had systemic chemotherapy within the last six weeks. 8. Subjects with renal failure on dialysis. 9. History of schistosomiasis. 10. Subjects who have had intervention (TURBT, diathermia, etc.,) following a previous cystoscopy.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Tri Valley Urology Medical Group Murrieta California
Durham VA Health Care System Durham North Carolina
The Urology Place San Antonio Texas

More Pacific Edge Limited trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05889195 on ClinicalTrials.gov ↗ ← All trials in the USA