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NCT02307552 · ClinicalTrials.gov registry record · NA

Transurethral Ultrasonic Imaging For Detection and Classification of Prostate Cancer

A NA study, sponsored by University of California, Irvine.

Terminated
Registry status
NA
Development phase
1
Enrollment target

NCT02307552 is a NA study that was terminated before completion, run by University of California, Irvine. The registered enrollment target is 1 participants.

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The verdict

NCT02307552, a NA study, was terminated before completion, sponsored by University of California, Irvine.

TERMINATED
Registry status
NA
Development phase
1 participants
Enrollment target

Study Summary

This study is being performed to verify the ability to use minimally invasive transurethral ultrasonic imaging technology for the purpose of identifying prostate cancer. Transurethral ultrasonic prostate imaging, may in the future, be used for detection and monitoring these disease processes to minimize the need for obtaining surgical biopsy specimens. The hypothesis is that tissue-density variations, as revealed in diagnostic ultrasonic imaging, results in unique image signatures for identification of prostate cancer. This imaging procedure provides a multifaceted view of the entire in-situ gland. The current use of Prostate Specific Antigen (PSA) for determining the likelihood of presence of cancer in the prostate gland requires interpretation and has a good but limited to predict prostate cancer on biopsy, with significant false prediction rates. More importantly as a blood test, the PSA test lacks the ability to pinpoint the location of the cancer within the prostate gland. Preliminary study findings have suggested that "Transurethral Ultrasonic Scanning" (TUUS) presents the desired improved diagnostic sensitivity for detection of cancer within the imaged prostate gland, and has the intrinsic capability to provide high resolution images of the transverse and future three-dimensional views of the entire gland better than currently used Transurethral Ultrasound (TRUS). Two important goals of the practicality of this minimally invasive technology will be assessed by this study. 1. The ability of TUUS to directly detect prostate cancer locations in the prostate. 2. The use of TUUS to successfully guide the prostate needle biopsy to cancer loci with a high rate accuracy.

Interventions

  • DEVICE UreScan

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2013-06
Est. Completion 2014-05
Phase NA

Sponsor

University of California, Irvine

368 total trials

What the Registry Record Tells You About NCT02307552

The ClinicalTrials.gov registry entry for NCT02307552 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Irvine, which has 368 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which UreScan is the first listed.

NCT02307552 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02307552 about?

NCT02307552 is a clinical study titled "Transurethral Ultrasonic Imaging For Detection and Classification of Prostate Cancer". This study is being performed to verify the ability to use minimally invasive transurethral ultrasonic imaging technology for the purpose of identifying prostate cancer. Transurethral ultrasonic prostate imaging, may in the future, be used for detection and monitoring these disease processes to mini...

What is the current status of trial NCT02307552?

This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2013-06. Estimated completion is 2014-05.

What interventions are being tested in trial NCT02307552?

The interventions under investigation include: UreScan (DEVICE).

Who is sponsoring clinical trial NCT02307552?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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