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Not listed No phase listed Observational

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

ClinicalTrials.gov ID: NCT00966095

Public ClinicalTrials.gov record NCT00966095. 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 Oct 18, 2026, 12:26 AM 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, Multi-Center PRostate Cancer Individual Signature Evaluation Trial (PReCISE) in Patients Undergoing Scheduled Prostate Biopsy

Brief summary

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

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.

Study identification

NCT ID
NCT00966095
Recruitment status
Not listed
Study type
Observational
Phase
Not listed
Lead sponsor
Source MDx
Industry
Enrollment
1,200 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
40 Years and older
Sex
Male
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
Dec 2009 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Nov 25, 2010

Started 2009

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
San Bernardino Urological Associates San Bernardino California 92404 —
The Urology Center of Colorado Denver Colorado 80211 —
University of Chicago Medical Center Chicago Illinois 60637 —
Johns Hopkins University Brady Urological Institute Baltimore Maryland 21287 —
Brigham and Women's Hospital/ Dana Farber Cancer Institute Brigham and Women's Hospital Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Bay State Clinical Trials Watertown Massachusetts 02472 —
University of Michigan Ann Arbor Michigan 48105 —
Karmanos Cancer Institute Wayne State University Detroit Michigan 48201 —
Mayo Clinic Rochester Minnesota 55905 —
University Urology Associates New York New York 10016 —
Mount Sinai Medical Center New York New York 10029 —
Durham VA Medical Center Durham North Carolina 27705 —
Duke University Medical Center Durham North Carolina 27710 —
Urology Clinics of North Texas Dallas Texas 75231 —
Urology San Antonio Research San Antonio Texas 78229 —
University of Washington Department of Urology Seattle Washington 98195 —

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 NCT00966095, 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 Nov 25, 2010 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00966095 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →