Under construction – not a live service
Sign in
Taking people in CanadaNo phase

Studies men with prostate cancer on active surveillance to find markers

Looks for markers that tell aggressive prostate cancers apart from slow-growing ones.

Plain-language title generated from the registry record
Registry title: Prostate Active Surveillance Study

Key facts

Where
Vancouver, CanadaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for men with early prostate cancer who have chosen active surveillance (close monitoring) instead of treatment right away.

Age
21 years or older
Sex
Men only
Disease stage
Prostate cancer confirmed by biopsy, limited to the prostate (T1-2, NX or N0, MX or M0). Diagnosis no more than 3 years before the baseline visit. No more than two biopsies, each with at least 10 cores.
Earlier treatment
No previous treatment for prostate cancer (no hormone therapy, radiation, surgery or chemotherapy).

Main reasons for not taking part

  • Unwilling or unable to have repeated prostate biopsies
  • Other cancers in the past, except adequately treated non-melanoma skin cancer, adequately treated superficial bladder cancer (Ta), or other solid tumors treated to remove all disease with no sign of disease for more than 5 years

Read by machine on 9 November 2026.

Where in Canada

  • University of British ColumbiaVancouver, CanadaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Washington
Trial code
NCT00756665
Record updated
2 September 2026
Original description
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.Read full original descriptionShow less

Canary Prostate Active Surveillance Study

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.

Inclusion: Histologically confirmed adenocarcinoma of the prostate from a prostate biopsy; Clinically localized prostate cancer: T1-2, NX or N0, MX or M0; No previous treatment for prostate cancer (including hormonal therapy, radiation therapy, surgery, or chemotherapy); ECOG Performance Status 0 or 1; Patient has elected Active Surveillance as preferred management plan for prostate cancer; Patient consent has been obtained according to local Institutional Review Board for acquisition of research specimens; Patient is accessible and compliant for follow-up; Prostate cancer diagnosis cannot be more than 3 years prior to baseline visit date; No more than two prostate biopsies including the initial biopsy in which cancer was diagnosed; If cancer diagnosis is more than one year before enrollment, there must be two prostate biopsies including the initial biopsy in which cancer was diagnosed and a subsequent biopsy. The subsequent biopsy may occur on the same day as the baseline visit; Biopsies must have at least 10 cores.

Exclusion: History of other malignancies, except: adequately treated non-melanoma skin cancer or adequately treated superficial bladder cancer (Ta) or other solid tumors curatively treated with no evidence of disease for > 5 years; Unwillingness or inability to undergo serial prostate biopsy.

ClinicalTrials.gov NCT00756665