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COMPLETED

The Cxbladder Monitoring Study

NCT02700659 · View on ClinicalTrials.gov ↗

Study Summary

The aim of this trial is to determine the performance characteristics of the Cxbladder test for the detection of recurrent urothelial carcinoma (UC) in patients with a recent history of urinary tract UC, who have been treated according to standard practice and are undergoing routine investigative cystoscopy. The gold standard for determination of clinical truth is cystoscopy, plus any follow up investigations relating to the current visit.

Conditions Studied

Interventions

  • OTHER Cxbladder

Study Locations (11)

New York

  • Premier Medical Group of the Hudson Valley — Kingston
  • Weill Cornell Medical College, Department of Urology — New York
  • Premier Medical Group of the Hudson Valley — New York
  • Premier Medical Group of the Hudson Valley — Newburgh

Alabama

  • Urology Centers of Alabama — Homewood

Connecticut

  • Urology Center of Grove Hill, One Lake Street — New Britain

Florida

  • Florida Urology Associates — Orlando

Idaho

  • Idaho Urologic Institute — Meridian

New Jersey

  • Delaware Valley Urology, LLC — New Jersey

Pennsylvania

  • Penn State Hershey Medical Center and College of Medicine — Hershey

Texas

  • UT Southwestern Medical Center — Dallas

Trial Details

FieldValue
Enrollment Target 803 participants
Start Date 2013-02-04
Est. Completion 2016-09-23

Sponsor

Pacific Edge Limited

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02700659

The ClinicalTrials.gov registry entry for NCT02700659 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 803 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pacific Edge Limited, which has 33 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 Urothelial Carcinoma appearing as the primary indexed condition, and to 1 intervention — of which Cxbladder 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: NCT02700659 reports 11 study locations spanning 8 distinct geographic areas — top geographies include New York, Alabama, Connecticut. 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 NCT02700659 about?

NCT02700659 is a clinical study titled "The Cxbladder Monitoring Study". The aim of this trial is to determine the performance characteristics of the Cxbladder test for the detection of recurrent urothelial carcinoma (UC) in patients with a recent history of urinary tract UC, who have been treated according to standard practice and are undergoing routine investigative cy...

What is the current status of trial NCT02700659?

This trial is currently completed. The enrollment target is 803 participants. The study started on 2013-02-04. Estimated completion is 2016-09-23.

What conditions does trial NCT02700659 study?

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

What interventions are being tested in trial NCT02700659?

The interventions under investigation include: Cxbladder (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02700659?

This trial is sponsored by Pacific Edge Limited, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02700659 being conducted?

This trial has 11 study locations across Alabama, Connecticut, Florida, Idaho, New Jersey. 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