Bladder EpiCheck Product Development Study for Bladder Cancer

This study is developing a new diagnostic test called Bladder EpiCheck. This test uses a urine sample to help detect bladder cancer or monitor for its return in people who have had it before. We are looking for 1000 participants aged 22 or older who are suspected of having bladder cancer or are undergoing surveillance for non-muscle invasive bladder cancer (NMIBC). The main goal is to collect urine samples to help improve the Bladder EpiCheck test. This is an observational study, meaning you won't receive a new treatment, but your samples will help develop a new diagnostic tool.

Study design
This is an observational study planning to enroll 1000 participants. It is not testing a treatment, but rather collecting information to develop a diagnostic test.
What's involved
You would have a single visit where you sign a consent form and provide a urine sample. Information about your demographics and any pathology results will also be collected.
Compensation
Not stated in the trial record.
Follow-up
The primary objective is measured at 1 year, but the record does not specify if participants have follow-up visits after the initial single visit.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07514143

Bladder EpiCheck Product Development Study

Recruiting
Not specifiedAges 22+Observational
Nucleix Ltd.
~1,000 participants
Updated 2026-04-07 on ClinicalTrials.gov
What's tested:Bladder EpiCheck

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
The primary objective of the study is to support the Bladder EpiCheck product development studies. There is no measurable endpoint for this study.
Measured over 1 year
Suspicion of Bladder Cancer
NMIBC Surveillance

NCT07514143

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Chesapeake Urology Research Associates

    Towson, Marylandstudy coordinator listed

    Recruiting

  • Om Research LLC

    San Diego, Californiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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  • The primary objective of the study is to support the Bladder EpiCheck product development studies. There is no measurable endpoint for this study.1 year

    The primary objective of the study is to support the Bladder EpiCheck product development studies. There is no measurable endpoint for this study. For each product development protocol a pre-specified primary endpoint will be defined in a dedicated SAP. For example, validation of a new PCR platform will assess the rate of agreement between the approved PCR platform and the new new platform.