Curcumin Biomarkers

Completed · Phase 1

Conditions studied: Colorectal Cancer

In brief

Colorectal cancer is a major problem in the United States and other developed countries. A safe and effective chemopreventive agent could reduce the burden of colorectal neoplasia. Curcumin, is a product that is derived from Curcuma longa. It has been used for thousands of years as a traditional remedy. Curcumin blocks a number of targets involved in tumor initiation, promotion, and progression, and is considered a promising chemopreventive agent. The investigators propose to enroll 40 patients after screening colonoscopy who will have rectal biopsies at baseline and after 4 weeks of curcumin 4 grams per day. The investigators will use microarray analysis to identify genes that are modified by curcumin that could be used as biomarkers in future chemoprevention studies. The study will also evaluate tolerability and toxicity.

Key facts

Study ID

NCT01333917

Run by

University of North Carolina, Chapel Hill

People needed

40

Starts

2010-11-01

Expected to finish

2013-01-01

Last updated by the study team

2013-02-07

Who can join

Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 40 - 80.
• A willingness to follow the study protocol, as indicated by provision of informed consent to participate
• Good general health

You may not qualify if…

• Familial colorectal cancer syndromes (e.g. Hereditary Non-Polyposis Colon Cancer, Familial Adenomatous Polyposis)
• Ulcerative colitis or Crohn's disease.
• History of large bowel resection for any reason
• Diagnosed narcotic or alcohol dependence
• Unwillingness to forgo curcumin/turmeric-containing supplements during the trial or consumption of curry/turmeric at meals > 3 times a week.
• Allergy to turmeric/curcumin.
• Women with childbearing potential who do not agree to practice effective birth control.
• Individuals with creatinine, AST or ALT above 1.5 times the upper limit of normal at baseline.
• Personal or inherited bleeding disorders or therapeutic anti-coagulation with warfarin.
• Women who are pregnant or nursing.
• Individuals who have taken antibiotics within the three months prior to enrollment.

Where it is running

• UNC Department of Family Medicine — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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