Extracellular Vesicle Analysis for Prostate Cancer

CT
Overseen ByClinical Trials Referral Office
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Mayo Clinic
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial examines how prostate cancer treatment affects certain particles in the blood and urine. These particles, known as extracellular vesicles, might indicate how well a patient responds to prostate cancer surgery. The trial collects samples from both prostate cancer patients and female volunteers for comparison. Men with high-risk prostate cancer, such as those with a PSA level over 20 or a Gleason score of 8 or higher, might be suitable candidates. As a Phase 2 trial, this research measures the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to important advancements in prostate cancer treatment.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

Why are researchers excited about this trial?

Researchers are excited about this trial because it aims to understand the baseline levels of prostate cancer-derived extracellular vesicles after local treatment. Unlike traditional treatments that focus on directly targeting cancer cells, this study looks at tiny particles released by prostate cancer cells to see how they change after treatment. By analyzing blood and urine samples, scientists hope to uncover new insights into how prostate cancer behaves and potentially develop new markers for monitoring the disease. This could lead to more personalized and effective treatment strategies in the future.

Who Is on the Research Team?

ED

Eugene D. Kwon, M.D.

Principal Investigator

Mayo Clinic in Rochester

Are You a Good Fit for This Trial?

Inclusion Criteria

I am 18 years old or older.
I understand the study and can agree to participate.
I have prostate cancer.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pre-surgery

Blood and urine samples are collected from prostate cancer patients before radical prostatectomy

Baseline

Post-surgery

Blood and urine samples are collected once post-surgery, 6 weeks to 6 months after surgery

6 weeks to 6 months

Follow-up

Annual blood collection for ongoing monitoring of prostate cancer-derived EV levels

Annual

What Are the Treatments Tested in This Trial?

Interventions

  • Non-Interventional Study

How Is the Trial Designed?

3

Treatment groups

Experimental Treatment

Group I: Observational (Cohort III)Experimental Treatment1 Intervention
Group II: Observational (Cohort II)Experimental Treatment1 Intervention
Group III: Observational (Cohort I)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Mayo Clinic

Lead Sponsor

Trials
3,427
Recruited
3,221,000+