| Registry | NCT03193541 |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Enrollment | 900 (Estimated) |
| Sponsor | Cedars-Sinai Medical Center (Other); collaborators: Nonagen Bioscience Corporation, Nara Medical University, University of California, Los Angeles, University of Rochester, National Cancer Institute (NCI), University of Texas, Southwestern Medical Center at Dallas, VA Long Beach Healthcare System, Nara Prefecture Seiwa Medical Center, University of Hawaii Cancer Research Center, Fred Hutchinson Cancer Center, Hoag Memorial Hospital Presbyterian |
| Conditions | Bladder Cancer |
| Dates | start 2016-12-30, primary completion 2029-02-01 (estimated), completion 2029-02-01 (estimated), first posted 2017-06-20, last updated 2026-02-04 |
| Locations | 8 sites in United States, Japan |
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To improve upon the non-invasive detection of BCa by further validating a multiplex ELISA assay directed at a BCa-associated diagnostic signature in voided urine samples of patients with microscopic hematuria.
Hematuria is the most common presentation of BCa with 8% of patients with microscopic hematuria harboring BCa. VUC is the most widely used urine-based assay for detecting BCa; however, it fails to detect approximately 50% of low-grade or early stage BCa when it is most curable. Because of this severe limitation, patients with hematuria will undergo an invasive examination of the urinary bladder, where a miniature camera is inserted into the bladder.
We propose to improve the non-invasive detection of BCa by further validating a multiplex ELISA assay directed at a BCa-associated diagnostic signature in voided urine samples of patients with microscopic hematuria.
Sex: All, ages: 18 Years to 90 Years
Inclusion Criteria: * Age 18 years or older * Have documented or reported microscopic hematuria within 3 month of study enrollment * Willing and able to give written informed consent Exclusion Criteria (participants must not): * Have history of BCa * History of previous cancer (excluding basal and squamous cell skin cancer) * Have a known active urinary tract infection or urinary retention * Have active stone disease (renal or bladder) or renal insufficiency (creatinine >2.0 mg/dL) * Have ureteral stents, nephrostomy tubes or bowel interposition * Have recent genitourinary instrumentation (within 10 days prior to signing consent) * Be unable or unwilling to complete the hematuria evaluation (i.e., cystoscopy and upper tract imaging)
| Facility | City | Country | Status |
|---|---|---|---|
| VA Long Beach Healthcare System | Long Beach, California | United States | Recruiting |
| Cedars-Sinai Medical Center | Los Angeles, California | United States | Recruiting |
| UCLA Medical Center | Los Angeles, California | United States | Recruiting |
| Hoag Memorial Hospital Presbyterian | Newport Beach, California | United States | Recruiting |
| University of Rochester Medical Center | Rochester, New York | United States | Recruiting |
| UT Southwestern Medical Center at Dallas | Dallas, Texas | United States | Recruiting |
| Nara Prefecture Seiwa Medical Center | Nara, Nara | Japan | Recruiting |
| Nara Medical University | Nara | Japan | Recruiting |
NIH grants: R01CA198887