Adjuvant Curcumin to Assess Recurrence Free Survival in Patients Who Have Had a Radical Prostatectomy
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- yair lotan
- Study ID
- NCT02064673
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 30 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Curcumin — DRUGCurcumin or placebo 500mg by mouth twice a day for 6 months
- placebo — DRUGplacebo orally twice a day
Study Details
This is a prospective study to determine if the adjuvant use of Curcumin improves recurrence-free survival.
Key Dates
- Start date
- May 31, 2014
- Status verified
- Mar 2026
- Primary completion
- Jun 30, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 650 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Active Comparator: CurcuminCurcumin 500 mg orally twice a day
- Placebo Comparator: sugar pillplacebo orally twice a day
Primary Outcome Measure
Serum prostate specific antigen [ Time Frame: 3 years ]
Central Contacts
- Corey Nixon214-645-8787
- Catherine Robinson214-645-8787
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UT Southwestern Medical Center | Dallas | Texas | 75390 | Yair Lotan, MD (PRINCIPAL_INVESTIGATOR) |
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