Prostate Cancer Prospective Cohort
2 other identifiers
observational
1,937
1 country
1
Brief Summary
The overall purpose of this research is to determine if certain genes increase the chance of developing prostate cancer and once diagnosed increase the chance of the prostate cancer spreading to other parts of the body.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2000
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2000
CompletedFirst Submitted
Initial submission to the registry
July 10, 2009
CompletedFirst Posted
Study publicly available on registry
July 13, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2027
December 17, 2025
December 1, 2025
27.1 years
July 10, 2009
December 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Ability to recognize increased risk of metastatic prostate cancer based on specific genetic polymorphisms.
At the time of prostate cancer diagnosis
Secondary Outcomes (1)
Ability to predict risk for treatment failure based on analysis of specific polymorphisms.
At the time of prostate cancer diagnosis
Study Arms (1)
Newly diagnosed patients
Patients with newly diagnosed prostate cancer.
Eligibility Criteria
Patients with newly diagnosed prostate cancer are being recruited for this study from Siteman Cancer Center radiation oncology, medical oncology and urology clinics.
You may qualify if:
- Newly diagnosed patients: 1. newly diagnosis of prostate cancer 2. untreated except for neoadjuvant systemic therapy.
You may not qualify if:
- Newly diagnosed patients: 1. inability to give informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Washington University School of Medicinelead
- Johns Hopkins Universitycollaborator
- National Cancer Institute (NCI)collaborator
- Wake Forest Universitycollaborator
Study Sites (1)
Washington University School of Medicine
St Louis, Missouri, 63110, United States
Biospecimen
Whole blood, serum, white cells, prostate tissue.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Bettina Drake, PhD
Washington University School of Medicine
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 10, 2009
First Posted
July 13, 2009
Study Start
May 1, 2000
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
June 1, 2027
Last Updated
December 17, 2025
Record last verified: 2025-12