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COMPLETED NA

The Efficacy of the Bladder EpiCheck for Detection of Recurrent Urothelial Cell Carcinoma

NCT02700464 · View on ClinicalTrials.gov ↗

Study Summary

Clinical trial to determine the efficacy (sensitivity and specificity) of the Bladder EpiCheck test compared to the gold standard cystoscopy and pathology in patients under monitoring for recurrence of bladder cancer.

Conditions Studied

Interventions

  • DEVICE Bladder EpiCheck Urine Test
  • PROCEDURE Cystoscopy and pathology

Study Locations (11)

Colorado

  • The Urology Center of Colorado — Denver

Maryland

  • Chesapeake Urology Research Associates — Baltimore

Michigan

  • Michigan Institute of Urology, P.C. — Troy

Minnesota

  • Metro Urology — Woodbury

New York

  • Urological Surgeons of Long Island — Garden City

North Carolina

  • Duke University Health System — Durham

Ohio

  • Cleveland Clinic — Cleveland

Tennessee

  • Vanderbilt University Medical Center — Nashville

Trial Details

FieldValue
Enrollment Target 680 participants
Start Date 2016-09
Est. Completion 2020-07
Phase NA

Sponsor

Nucleix

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02700464

The ClinicalTrials.gov registry entry for NCT02700464 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 680 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nucleix, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Bladder Cancer appearing as the primary indexed condition, and to 2 interventions — of which Bladder EpiCheck Urine Test is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02700464 reports 11 study locations spanning 11 distinct geographic areas — top geographies include Colorado, Maryland, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02700464 about?

NCT02700464 is a clinical study titled "The Efficacy of the Bladder EpiCheck for Detection of Recurrent Urothelial Cell Carcinoma". Clinical trial to determine the efficacy (sensitivity and specificity) of the Bladder EpiCheck test compared to the gold standard cystoscopy and pathology in patients under monitoring for recurrence of bladder cancer.

What is the current status of trial NCT02700464?

This trial is currently completed. It is a NA study. The enrollment target is 680 participants. The study started on 2016-09. Estimated completion is 2020-07.

What conditions does trial NCT02700464 study?

This clinical trial studies the following conditions: Bladder Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02700464?

The interventions under investigation include: Bladder EpiCheck Urine Test (DEVICE), Cystoscopy and pathology (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02700464?

This trial is sponsored by Nucleix, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02700464 being conducted?

This trial has 11 study locations across Colorado, Maryland, Michigan, Minnesota, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial