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NCT Number: NCT03193541

A Novel Multiplex ELISA Assay for Evaluating Patients With Microscopic Hematuria for Bladder Cancer

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.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Nara Prefecture Seiwa Medical Center, Nara, Japan

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About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Primary outcomes

  1. Sensitivity and specificity of multiplex ELISA assay will be confirmed by cystoscopy.

    Time frame: 1 year

Secondary outcomes

  1. Sensitivity and specificity of multiplex ELISA assay will be compared to VUC and NMP-22 BladderChek.

    Time frame: 1 year

Study contacts

Contact information is provided by the study sponsor or research team.

Charles Rosser, MD

CONTACT

[email protected]

310-423-5609

Sponsors and collaborators

Lead sponsor

Cedars-Sinai Medical Center

Other

Collaborators

  • Fred Hutchinson Cancer Center
  • Hoag Memorial Hospital Presbyterian
  • Nara Medical University
  • Nara Prefecture Seiwa Medical Center
  • National Cancer Institute (NCI)
  • Nonagen Bioscience Corporation
  • University of California, Los Angeles
  • University of Hawaii Cancer Research Center
  • University of Rochester
  • University of Texas, Southwestern Medical Center at Dallas
  • VA Long Beach Healthcare System

Registry information

Important dates

Study start
2016
Primary completion
2029
Study completion
2029
First posted
Jun 20, 2017
Registry last updated
Feb 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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