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Recruiting

NCT Number: NCT02064673

Adjuvant Curcumin to Assess Recurrence Free Survival in Patients Who Have Had a Radical Prostatectomy

This is a prospective study to determine if the adjuvant use of Curcumin improves recurrence-free survival.

Recruiting

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Key information

Age range

30 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 3

Primary location

About this study

This is a prospective study to determine if the adjuvant use of Curcumin improves recurrence-free survival in patients after radical prostatectomy compared to placebo

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Status post radical prostatectomy for histologically confirmed adenocarcinoma of the prostate
  • pathologically confirmed T1-T3 disease
  • no sign of lymph node or metastatic disease
  • pT1-pT3pNxMx patients in whom standard NCCN or AUA guidelines would suggest are at low risk for pelvic lymph node or metastatic disease and who would not require confirmatory imaging for metastatic disease. This includes patients with Gleason 6 or 7(T2 disease) and PSA less than 20.
  • Eastern Cooperative Oncology Group(ECOG) status 0-2
  • adequate renal and liver function as well as bone marrow reserve (measured serum creatinine <2mg/dl, bilirubin ≤ 1.5 mg/dl, ANC ≥ 1.5 x 10 (3) uL, platelets ≥ 50 x K/uLL, and hemoglobin ≥ 10 g/dL)
  • 30-80 y/o at time of diagnosis with a life expectancy of >= 3 yrs
  • focally positive surgical margins are permitted
  • no plan to receive adjuvant hormone or radiation therapy
  • PSA at the time of enrollment must be undetectable
  • life expectancy of 3 years

Exclusion criteria

  • must not have exceeded 3 months from time of surgery to enrollment into study
  • T3b or T4 or node positive disease
  • macroscopic residual disease after surgery
  • hormone therapy before surgery
  • history of gallbladder problems or gallstones, or biliary obstruction, unless patient had cholecystectomy
  • radiation therapy as primary treatment after surgery
  • INR value greater than 1.5
  • AST/ALT are equal or greater than 2 times the upper limit of normal
  • antiplatelet or anticoagulant agents- patients taking 81mg of Aspirin will be allowed with close observation
  • history of gastric or duodenal ulcers or untreated hyperacidity syndromes
  • patients who are currently taking curcumin and are unwilling to stop or plan to take curcumin during the study

Treatment and study plan

curcumin

Drug

Curcumin or placebo 500mg by mouth twice a day for 6 months

Other names: Bio-Curcumin(BCM-95CG), Tumeric

Placebo

Drug

placebo orally twice a day

Other names: sugar pill

Primary outcomes

  1. Serum prostate specific antigen

    Time frame: 3 years

    Recurrence free survival defined as a total serum prostate specific antigen of <0.2ng/ml.

Study contacts

Contact information is provided by the study sponsor or research team.

Catherine Robinson

CONTACT

[email protected]

214-645-8787

Corey Nixon

CONTACT

[email protected]

214-645-8787

Sponsors and collaborators

Lead sponsor

yair lotan

Other

Registry information

Official study title

Randomized Trial of Adjuvant Curcumin After Prostatectomy

Important dates

Study start
2014
Primary completion
2028
Study completion
2028
First posted
Feb 17, 2014
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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