Curcumin (Tumeric) in the Treatment of Irritable Bowel Syndrome: A Randomized-Controlled Trial (CuTIBS)

Kaiser Permanente

Status and phase

Completed

Phase 4

Conditions

Irritable Bowel Syndrome

Treatments

Dietary Supplement: curcumin

Dietary Supplement: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00779493

4893

Details and patient eligibility

About

Evidence exists to support low-grade inflammation as the inciting factor leading to visceral hypersensitivity and alteration in motility in irritable bowel syndrome.In the medical literature,there is ample in vitro and in vivo evidence supporting turmeric and its derivative curcumin as an antitumor, anti-inflammatory and antioxidant agent. We propose a randomized, placebo-controlled, double blinded, parallel treatment study evaluating the effects of turmeric on the symptoms of irritable bowel syndrome.

Enrollment

17 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients from the hospitals and clinics of the Southern California Permanente Medical Group who conform to the Rome III criteria and

Age 18 years and above,
Male or female,
Able to give consent and follow the treatment plan and be able to answer surveys.
Negative serum pregnancy test (females of childbearing potential only) and are willing to use an adequate method of contraception throughout the duration of the study.

Exclusion criteria

Any of the following: diabetes, HIV disease, use of anticoagulants or antiplatelet medication, abnormal coagulation or thrombocytopenia, biliary obstruction, inflammatory bowel, symptomatic gallstones, celiac disease, ongoing use of medications known to cause or exacerbate symptoms of IBS and chronic, daily users of IBS medications.
Use of scheduled IBS medications for 4 weeks prior to and during the treatment period.