Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseobservationalRules rewrite
Care of the Prostate Cancer Patient and Prospective Procurement of Prostate Cancer Tissue
Background: Prostate cancer is the most common noncutaneous cancer among men in the U.S. Researchers want to study blood, tissue, and fluid samples of people with prostate cancer.
This is an observational study. You are not assigned a new experimental drug. Researchers measure what already happens in your care or in daily life.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
This listing is observational (StudyType). The registry does not assign a new experimental drug as the study intervention.
They plan to enroll about 3,000 people at Bethesda. Taking part typically means study visits and measurements plus check-ins.
Official title (unrewritten)
Care of the Prostate Cancer Patient and Prospective Procurement of Prostate Cancer Tissue
Primary outcome (registry wording): Collect samples for the purpose of studying the molecular mechanisms of carcinogenesis in prostate cancer
Who it is for (from inclusion criteria)
Ages 18 Years to any
Men only
how well you can do daily activities (ECOG score) of 0-2
PSA \> or equal to 1.0 ng/ml (for patients aged 30 - 49 years) OR
PSA \> or equal to 2.5 ng/ml (for patients 50 years or older) OR
Abnormal DRE (i.e. enlarged, asymmetric, nodular, firm or tender) OR
Abnormal prostate MRI finding OR
Family history of first degree relatives (brother or father) with prostate cancer or first-degree relatives (mother or sister) with breast or ovarian cancer
Who the registry excludes
1\. Subjects whose comorbidities would preclude diagnostic or therapeutic intervention
This study will collect blood from patients with cancer to study the level of cells which decrease the immune response (suppressor cells) before and after chemotherapy. Patients 18 years of age and older with cancer may participate.
This study will investigate what causes hereditary leiomyomatosis renal (kidney) cell cancer, or HLRCC, and how the disease is related to the development of kidney tumors. Leiomyomas are benign (non-cancerous) tumors arising from smooth muscle.
This study aims to provide long-term follow-up care of patients previously enrolled in a vaccine study that involved poxviral vectors. Vectors are sequences of genetic material that can be used to introduce specific genes into genetic makeup.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT02594202?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT02594202?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.