Prostate Active Surveillance Study

NCT00756665 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2026-01-15

No results posted yet for this study

Summary

The Prostate Active Surveillance Study (PASS) is a research study for men who have chosen active surveillance as a management plan for their prostate cancer. Active surveillance is defined as close monitoring of prostate cancer with the offer of treatment if there are changes in test results. This study seeks to discover markers that will identify cancers that are more aggressive from those tumors that grow slowly.

Conditions

  • Prostatic Neoplasms

Sponsors & Collaborators

  • Canary Foundation

    collaborator OTHER
  • Early Detection Research Network

    collaborator NETWORK
  • University of Washington

    lead OTHER

Principal Investigators

  • Daniel W. Lin, MD · University of Washington

  • James D. Brooks, MD · Stanford University

  • Martin E. Gleave, MD · University of British Columbia

  • Michael Liss, MD · University of Texas Health Science Center San Antonio

  • Peter R. Carroll, MD, MPH · University of California, San Francisco

  • Robert W. Given, MD · Eastern Virginia Medical School

  • Andrew A Wagner, MD · Beth Israel Deaconess Medical Center/Harvard Medical School

  • Todd M. Morgan, MD · University of Michigan

  • Lisa F Newcomb, PhD · Fred Hutchinson Cancer Research Center/University of Washington

  • Martin G. Sanda, MD · Emory University

  • Matthew R. Cooperberg, MD, MPH · Veterans Affairs San Francisco Health Care System

  • Atreya Dash, MD · Veterans Affairs Puget Sound Health Care System

Eligibility

Min Age
21 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2029-09-30
Completion
2032-09-30

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00756665 on ClinicalTrials.gov