Actively Recruiting
Real World Prostate Cancer Registry
Led by Cincinnati Cancer Advisors · Updated on 2025-05-31
1000
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Prostate cancer is the most common cancer diagnosed in men in the USA with 268,490 cases diagnosed in 2022 constituting 27% of male cancers and 34,500 deaths (11%) occurred in same year.1 Prostate cancer is a very heterogeneous disease that has different presentations, molecular and pathological features, stages, and disease biology. The treatment options are dependent on the disease stage, its features, and the patient's condition and preferences. The disease outcome also varies significantly due to the previous heterogeneity of the features in addition to other social determinants of health. Therefore, it is critical to obtain real-world data that reflects the actual patterns of prostate cancer presentation, work up, management, and outcome. Real World Prostate Cancer Registry (RWPCR) aims at compiling real world data from patients presented with prostate cancer in the tristate area. The data collection will be prospective and longitudinal including patients' demographics and disease characteristics, work up, management, and outcome.
CONDITIONS
Official Title
Real World Prostate Cancer Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients with pathologically confirmed primary prostate cancer
- Diagnosis since January 1st, 2023
- Acceptance to sign the consent form
- 18 years old or older
- Resident of Ohio, Kentucky or Indiana
You will not qualify if you...
- Having diagnosis of other cancer except squamous cell cancer of the skin
- Refusal to sign a consent form
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cincinnati Cancer Advisors
Cincinnati, Ohio, United States, 45212
Actively Recruiting
Research Team
A
Abdul Jazieh, MD, MPH
CONTACT
A
Amy Barber
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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