Purpose

The goal of this observational study is to test whether the ExoDx Prostate test add value in biopsy decision making to patients with prostate cancer on an active surveillance regimen.

Condition

Eligibility

Eligible Ages
Over 45 Years
Eligible Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male, 45+ years of age diagnosed with low-grade or favorable-intermediate prostate cancer and on an active surveillance regimen

Exclusion Criteria

  • Clinical symptoms of urinary tract infection at time of enrollment. - History of invasive treatment for benign prostatic hypertrophy with in 6 months of enrollment. - Known hepatitis or HIV - History of concurrent renal/bladder tumors

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

Chesapeake Urology
Towson, Maryland 21204
Contact:
Emily Ayre

More Details

NCT ID
NCT05572099
Status
Unknown status
Sponsor
Exosome Diagnostics, Inc.

Study Contact

Sonia Kumar, PhD
6175880500
Sonia.Kumar@bio-techne.com

Detailed Description

The current trial seeks to evaluate the role of the ExoDx Prostate test in men with low and favorable intermediate prostate cancer undergoing an active surveillance regimen.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.