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Completed Phase 3 Interventional Results available

A Study of Blue Light Flexible Cystoscopy With Cysview in the Detection of Bladder Cancer in the Surveillance Setting

ClinicalTrials.gov ID: NCT02560584

Public ClinicalTrials.gov record NCT02560584. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 9:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Open, Comparative, Within Patient Controlled Multicenter Phase 3 Study of Blue Light Cystoscopy With Cysview and White Light Cystoscopy Using KARL STORZ D-Light C PDD Flexible Videoscope System in Detection of Bladder Cancer in Patients With Bladder Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to investigate if blue light cystoscopy with Cysview improves detection of tumors in patients with bladder cancer during surveillance cystoscopy, using the KARL STORZ D-Light C PDD Flexible Videoscope System. Another purpose is to investigate if Cysview and blue light is safe and effective when used repeatedly.

Study identification

NCT ID
NCT02560584
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Photocure
Industry
Enrollment
304 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2015
Primary completion
Apr 4, 2017
Completion
Apr 4, 2017
Last update posted
Jul 1, 2018

2015 – 2017

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
USC Norris Comprehensive Cancer Center Los Angeles California 90033
University of Chicago Medical Center Chicago Illinois 60637
University of Iowa Iowa City Iowa 52242
Johns Hopkins University Baltimore Maryland 21205
University of Minnesota Minneapolis Minnesota 55455
NYU Langone Urology Associates New York New York 10016
Columbia University Medical Center New York New York 10032
Montefiore Medical Center The Bronx New York 10461
University of North Carolina, Department of Urology Chapel Hill North Carolina 27599
Ohio State University The James Cancer Hospital Columbus Ohio 43210
University of Oklahoma-Stephenson Cancer Center Oklahoma City Oklahoma 73104
Thomas Jefferson University Philadelphia Pennsylvania 10197
Vanderbilt University Medical Center Nashville Tennessee 37232
UT Southwestern Medical Center Dallas Texas 75390
MD Anderson Cancer Center Houston Texas 77030
Michael E. DeBakey VA Medical Center Houston Texas 77030
University of Wisconsin Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02560584, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 1, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02560584 live on ClinicalTrials.gov.

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