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.
Bladder EpiCheck Product Development Study
At a glance
Conditions
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.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- 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.