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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00718094
Other study ID # 390.05
Secondary ID 5K23DK073750
Status Completed
Phase Phase 2
First received July 16, 2008
Last updated November 14, 2017
Start date March 2008
Est. completion date April 2012

Study information

Verified date November 2017
Source University of Louisville
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Green tea consists of several components, with most research focusing on the polyphenol fraction. The polyphenol fraction(-)-epigallocatechin-3-gallate (EGCG)has been studied extensively as an anti-inflammatory agent as well as a preventative agent for cancer. It has been shown to effectively reduce the inflammation associated with animal models of inflammatory bowel disease. This clinical trial will determine the ability of EGCG, in the form of Polyphenon E®, to treat patients with mild to moderately severe ulcerative colitis.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2012
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Adult male or female with mildly to moderately active ulcerative colitis

Exclusion Criteria:

- Off prohibited medications for proscribed period of time

- Evidence of infectious colitis

- Labs outside of range

- Pregnancy or lactation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Polyphenon E®
Oral capsules
Placebo Oral Tablet
Oral tablet: placebo

Locations

Country Name City State
United States University of Louisville Clinical Research Center Louisville Kentucky

Sponsors (2)

Lead Sponsor Collaborator
University of Louisville National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Dryden GW, Lam A, Beatty K, Qazzaz HH, McClain CJ. A pilot study to evaluate the safety and efficacy of an oral dose of (-)-epigallocatechin-3-gallate-rich polyphenon E in patients with mild to moderate ulcerative colitis. Inflamm Bowel Dis. 2013 Aug;19(9 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Subjects With a Reduction in the Disease Activity Index of >3, or Clinical Remission. This Index is a measure of ulcerative colitis severity. The index assesses four variables, which include stool frequency, severity of bleeding, colonic mucosal appearance, and the physician's overall assessment of disease activity.
Each variable is scored from 0-3 so that the total index score ranges from 0-12; 0-2: remission; 3-6: mild; 7-10: moderate; >10: severe UC.
day 56