PRostate Cancer Individual Signature Evaluation Trial in Patients Undergoing Scheduled Prostate Biopsy

Status unconfirmed

Conditions studied: Prostate Cancer

In brief

The purpose of this study is to develop and validate a blood-based diagnostic test that will predict prostate biopsy outcome as positive or negative for prostate cancer. Such a test will serve to reduce the number of unnecessary prostate biopsies.

Key facts

Study ID

NCT00966095

Run by

Source MDx

People needed

1200

Starts

2009-12-01

Last updated by the study team

2010-11-25

Who can join

Age: 40 and older. Sex: male. Healthy volunteers: not accepted.

You may not qualify if…

• Unable or unwilling to provide informed consent

Where it is running

• San Bernardino Urological Associates — San Bernardino, California, United States
• The Urology Center of Colorado — Denver, Colorado, United States
• University of Chicago Medical Center — Chicago, Illinois, United States
• Johns Hopkins University Brady Urological Institute — Baltimore, Maryland, United States
• Brigham and Women's Hospital/ Dana Farber Cancer Institute — Boston, Massachusetts, United States
• Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
• Bay State Clinical Trials — Watertown, Massachusetts, United States
• University of Michigan — Ann Arbor, Michigan, United States
• Karmanos Cancer Institute Wayne State University — Detroit, Michigan, United States
• Mayo Clinic — Rochester, Minnesota, United States
• University Urology Associates — New York, New York, United States
• Mount Sinai Medical Center — New York, New York, United States
• Durham VA Medical Center — Durham, North Carolina, United States
• Duke University Medical Center — Durham, North Carolina, United States
• Urology Clinics of North Texas — Dallas, Texas, United States
• Urology San Antonio Research — San Antonio, Texas, United States
• University of Washington Department of Urology — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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