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Completed

NCT Number: NCT01360320

Minimizing the Risk of Metachronous Adenomas of the Colorectum With Green Tea Extract -MIRACLE-

This is a randomized, placebo controlled, multicentric trial to investigate the effect of diet supplementation with green tea extract containing 300mg epigallocatechin gallate (EGCG), the major polyphenol of green tea, on the recurrence of colon adenomas.

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Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ostalb-Klinikum Aalen, Medizinische Klinik 1, Sekretariat Prof. Kleber, Aalen, Germany

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About this study

Prevention of colorectal cancer is a major health care issue because of the high incidence of this cancer. So far, pharmaceutical chemoprevention has not gained widespread acceptance due to side effects of the chemopreventive agents used. Nutraceuticals such as polyphenols from tea plants have demonstrated remarkable therapeutic and preventive effects in molecular, epidemiological and clinical trials. However, controlled trials demonstrating the efficacy of nutraceuticals fo the prevention of colorectal cancer are largely missing.

The investigators present this randomized, placebo controlled, multicentric trial to investigate the effect of diet supplementation with green tea extract containing 300mg epigallocatechin gallate (EGCG), the major polyphenol of green tea, on the recurrence of colon adenomas.

Patients who underwent polypectomy for colonic polyps will be randomized after a one month verum run-in period to receive either 150mg EGCG two times daily or placebo over the course of three years. The beneficial safety profile of decaffeinated green tea extract, the quantifiable and known active content EGCG, and the accumulating evidence on its cancer preventive potential require in our view a validation of this compound for the "nutriprevention" of colorectal adenoma. Good accessibility and low costs might render this nutraceutical a top candidate for a wider use as food supplement in colon cancer prevention.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Between 50-80 years of age
  • Histologically confirmed colorectal adenomas or serrated lesions removed during colonoscopy within the last 6 months
  • Good performance status (ECOG < 2) at study entrance
  • Written informed consent.

Exclusion criteria

  • History of hereditary nonpolyposis colorectal cancer (HNPCC) or familial adenomatous polyposis (FAP)
  • History of colon or rectal cancer, other concomitant cancers with the exemption of basalioma or curative treated cancers without actual anticancer medication.
  • Intestinal malabsorption, short bowel syndrome or surgical bowel interventions leading to malabsorption
  • Liver failure (hepatitis, cirrhosis, elevation of liver enzymes ALT, AST or bilirubin to more than 2.5 fold of the reference levels)
  • Inflammatory bowel disease
  • Regular intake of NSAIDs (also Cox2 inhibitors) for more than 3 months per year except of low-dose aspirin (100 mg per day)
  • Immunosuppressive medication
  • Impaired capacity to consent or who are impaired in swallowing a pill
  • Regular consumption of green tea extract as nutritional supplement (with a content of EGCG of more than 100mg per day) of longer than 6 months during the past two years
  • Allergic reactions towards green tea

Treatment and study plan

Green tea extract of Camellia Sinensis

Dietary Supplement

Powdered decaffeinated green tea extract of Camellia Sinensis, packed in hard gelatine capsules containing either 150 mg EGCG

  • Run-in period with 150mg EGCG two times daily (p.o) for 4 weeks
  • 150mg EGCG two times daily (p.o.) over the course of three years.
  • Colonoscopy after 3 years

Green tea extract of Camellia Sinensis followed by placebo

Dietary Supplement

Powdered decaffeinated green tea extract of Camellia Sinensis, packed in hard gelatine capsules containing either 150 mg EGCG

  • Run-in period with 150mg EGCG two times daily (p.o.) for 4 weeks
  • Placebo two times daily (p.o.) over the course of three years
  • Colonoscopy after 3 years

Primary outcomes

  1. Incidence of metachronous colorectal adenomas (tubulovillous, tubular, villous and serrated lesions) at the 3 year follow-up colonoscopy

    Time frame: 3 years

Secondary outcomes

  1. Occurrences of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  2. Number of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  3. Size of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  4. Localization of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  5. Histological subtypes of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  6. Invasive growth of colorectal adenomas or mucosal lesions

    Time frame: 3 years

  7. Incidence of colorectal carcinoma

    Time frame: 3 years

  8. Translational research

    Time frame: 3 years

    Genetic and biochemical biomarkers for recurrence of adenoma or development of dysplasia and carcinoma (blood samples and histological in tissue samples of the colorectal lesions)

  9. Toxicity and feasibility

    Time frame: 3 years

Sponsors and collaborators

Lead sponsor

Martin-Luther-Universität Halle-Wittenberg

Other

Collaborators

  • Deutsche Krebshilfe e.V., Bonn (Germany)
  • KKS Netzwerk
  • University of Ulm

Registry information

Acronym: MIRACLE

Important dates

Study start
2011
Primary completion
2019
Study completion
2019
First posted
May 25, 2011
Registry last updated
Sep 20, 2019

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.