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Prostate Cancer Screening and Dietary HA Exposure in African-Americans: Phase II
RATIONALE: Screening may help doctors find prostate cancer sooner, when it may be easier to treat. The amount of heterocyclic amines in the diet may affect prostate cancer screening results and the risk of prostate cancer. PURPOSE: This phase II trial is studying prostate cancer screening and dietary heterocyclic amines in African American men.
OBJECTIVES: * Estimate dietary heterocyclic amine (HA) exposure in African American men who use HA-forming meats and cooking methods. * Correlate dietary HA exposure with prostate-specific antigen and digital rectal exam screening results (i.e., higher HA exposure with increased abnormality in prostate cancer screening results) in these participants. OUTLINE: This is a prospective study. Participants complete a routine medical questionnaire and undergo a detailed dietary interview that focuses on meat consumption, cooking preferences, and other factors that may be associated with prostate cancer risk. Participants then undergo a digital rectal exam (DRE) and blood collection for prostate-specific antigen (PSA) testing (total PSA and % free PSA). Results of PSA testing and DRE, including follow-up instructions (if needed), are sent to the participant 3-4 weeks later. Blood samples are also examined by phenotypic assays for UV-damage induced nucleotide excision-repair capacity. PROJECTED ACCRUAL: A total of 800 participants will be accrued for this study.
Age
50 - 70 years
Sex
MALE
Healthy Volunteers
Yes
Lawrence Livermore National Laboratory at University of California
Livermore, California, United States
Alta Bates Summit Medical Center - Summit Campus
Oakland, California, United States
Start Date
March 1, 2002
Last Updated
September 20, 2013
800
ESTIMATED participants
physiologic testing
OTHER
study of socioeconomic and demographic variables
OTHER
evaluation of cancer risk factors
PROCEDURE
mutation carrier screening
PROCEDURE
study of high risk factors
PROCEDURE
Lead Sponsor
Lawrence Livermore National Laboratory at University of California
Collaborators
NCT05691465
NCT06842498
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04550494