Phase 3 Prostate Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have had a radical prostatectomy (surgical removal of the prostate) for confirmed prostate cancer
- People whose cancer was confirmed by a pathologist to be at stage T1, T2, or T3 (meaning the cancer was contained or had only limited spread beyond the prostate)
- People with no signs that the cancer has spread to the lymph nodes or other parts of the body
- People considered low risk for cancer spread to the lymph nodes, with a Gleason score of 6 or 7 (a measure of how aggressive the cancer appears), stage T2 disease, and a PSA level below 20 at the time of diagnosis
- People with a general health and activity level rated as ECOG 0–2 (meaning fully active to capable of basic self-care)
- People with healthy enough kidney function, liver function, and blood cell levels, as measured by specific lab tests (confirm with trial site for exact values)
- People aged 30 to 80 years old at the time of diagnosis, with a life expectancy of at least 3 years
- People whose surgical margins show only a small, limited area of cancer cells at the edge (focally positive margins)
- People who are not planning to receive hormone therapy or radiation therapy after surgery
- People whose PSA level is undetectable at the time of enrolling in the trial
Who may not be able to join:
- People who are more than 3 months past their surgery at the time of enrolling
- People whose cancer was confirmed as stage T3b, T4, or has spread to the lymph nodes
- People who had visible cancer remaining in the body after surgery
- People who received hormone therapy before their surgery
- People with a history of gallbladder problems, gallstones, or a blockage in the bile duct — unless the gallbladder has already been surgically removed
- People who are receiving radiation therapy as the main treatment after surgery
- People with a blood clotting measure (INR) greater than 1.5
- People with liver enzyme levels (AST/ALT) that are two or more times higher than the normal range
- People taking blood-thinning or anti-clotting medications (note: people taking low-dose aspirin at 81mg may be permitted with close monitoring — confirm with trial site)
- People with a history of stomach or duodenal ulcers, or untreated conditions causing excess stomach acid
- People who are currently taking curcumin supplements and are unwilling to stop, or who plan to take curcumin during the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Yair Lotan, MD, University of Texas Southwestern Medical Center
Phone: 214-645-8787
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Serum prostate specific antigen
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.