High Resolution Imaging for Early and Better Detection of Bladder Cancer
Completed
Conditions studied: Bladder Cancer
In brief
The goal of this study is to develop, optimize, and validate a High Resolution Imaging System in the bladder that displays images in real-time, providing automated diagnostic criteria for bladder cancer screening. High resolution images of normal bladder tissue and suspicious bladder lesions will be collected from patients who present to the study site for clinical evaluation.
Key facts
- Study ID
- NCT02340650
- Run by
- The University of Texas Health Science Center, Houston
- People needed
- 37
- Starts
- 2015-04-01
- Expected to finish
- 2020-09-30
- Last updated by the study team
- 2021-06-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with clinically suspicious bladder lesion or clinical finding; or who are undergoing cystoscopy as part of their routine clinical care.
- Must be willing and able to participate and provide written informed consent
- Women of childbearing age who have the possibility of being pregnant must have a negative pregnancy test prior to participation
You may not qualify if…
- Patient with sufficient evidence of cognitive impairment that limits the subject's ability to understand the protocol, provide informed consent, or to comply with the protocol procedures.
- Women with the possibility of having the pregnancy.
- Patients having acute infection.
- Person with Lidocaine sensitivity.
Where it is running
- Lyndon B. Johnson General Hospital — Houston, Texas, United States
Full record on ClinicalTrials.gov
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