Prostate cancer detection may soon be as simple as a urine test
NCT ID NCT02657863
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study collected blood and urine samples from 61 men with prostate cancer and healthy volunteers to look for cancer DNA. The goal is to develop a non-invasive way to detect and track prostate cancer without needing a biopsy. Researchers compared genetic material from cancer patients to healthy individuals to find differences that could lead to better diagnosis and treatment monitoring.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could lead to a simple, non-invasive test to detect and monitor prostate cancer using blood or urine samples.
- What could go wrong
- This is an early-stage observational study with only 61 participants, so results may not apply broadly. The approach is still experimental and may not prove reliable enough for clinical use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
61 people
The number who actually took part.
- Started
-
Nov 2014
- Finished
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Apr 2023
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Healthy volunteers and men with prostate cancer
- Ages
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18 to 100 years
- Sex
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Male participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male older than or equal to 18 years of age, but not older than 100 years of age. 2. Signed informed consent prior to initiation of any study-related procedures. 3. Minorities are included in this protocol. 4. Signed informed consent prior to initiation of any study-related Exclusion Criteria: 1. It is the enrolling study physician's discretion to decide if a patient is not fit enough to undergo procedures outlined in this protocol. 2. Persons who are incarcerated are not eligible to participate. 3. Women are not eligible. 4. Persons incapable of providing informed consent are not eligible. 5. Any person with a personal history of prior malignancy is not eligible 6. Persons with an inherited cancer syndrome or a medical history suggestive of an inherited cancer syndrome are not eligible.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Johns Hopkins SKCCC
Baltimore, Maryland, 21287, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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