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Dietary Factors in Prostate Cancer Screening
Study Summary
This trial is screening African American men for prostate cancer and studying how dietary heterocyclic amines affects screening results and prostate cancer risk.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Find a Location
Who is running the clinical trial?
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- I do not have any health issues that would stop me from joining the study.I want to be screened for prostate cancer as part of my routine health check.I am an African American male.I have never been diagnosed with prostate cancer.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Is this research project recruiting new participants?
"According to clinicaltrials.gov, this particular research endeavour is no longer accepting patients; the initial post was issued on March 1st 2002 and it has been modified as recently as September 19th 2013. Nevertheless, a variety of other medical trials are currently recruiting participants - 1321 in total."
What are the criteria for enrollment in this research project?
"This trial is seeking to enrol 800 individuals, aged between 50 and 70 years old, who have recently been diagnosed with prostate cancer. To be eligible for the study participants must not previously have had any diagnosis of this disease, possess no medical or physical disability that would stop them from participating in the experiment; hold a residence within close proximity Oakland, California."
Is this therapeutic option free from adverse effects?
"Due to a lack of clinical data documenting efficacy, the safety rating for this treatment was assessed as 2 on a scale of 1-3."
Is eligibility for this experiment limited to adults aged 18 or older?
"This study seeks participants aged between 50 and 70 years old."
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