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Completed

NCT Number: NCT02141945

Microbiome Test for the Detection of Colorectal Polyps and Cancer

The purpose if this study is to measure the sensitivity, specificity and accuracy of the Metabiomics Colon Polyp and Colorectal Cancer Assay for the non-invasive detection of colon polyps or colorectal cancer.

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Key information

Age range

45 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

DC Endoscopy Center, Washington D.C., District of Columbia, United States

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About this study

The purpose of this study is to conduct clinical research to investigate the association of the gut microbiome with colonic neoplasia. In this study patients will supply samples of their gut microbiome prior to scheduled colonoscopy; the relative abundance of microbes from those samples will be used to predict the presence or absence of colon polyps or colorectal cancer. Microbiome based predictions from blinded samples will be compared with colonoscopy and pathology results to quantify the sensitivity, specificity and accuracy (reported as %) of the Metabiomics Colon Polyp and Colorectal Cancer Assay for colon polyps. The limited sample size is anticipated to be insufficient to quantify sensitivity to colorectal cancer.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male or female,
  • Age: 45-80 years,
  • Patients undergoing polyp surveillance or screening colonoscopy who are ASA Class 1-3. No ASA Class 4 or 5 will be included.Footnote
  • All ethnic and racial groups will be included,
  • Able to comprehend, sign, and date the written informed consent form (ICF),
  • Able to give informed consent in English.

Exclusion criteria

  • History of Inflammatory Bowel Disease
  • Inability to schedule the colonoscopy within 60 days of the initial stool sample
  • Colonic pathology that in the opinion of the endoscopist could interfere with the accuracy of the colonoscopy. Examples include: colonic stricture, poor preparation, obstructing tumor.
  • ASA class 4 or greater
  • Vulnerable subjects. Students, nursing home residents, institutionalized patients, and those with psychological or physical incapacity.

Treatment and study plan

Primary outcomes

  1. Performance of Metabiomics Colon Polyp and Colorectal Cancer Assay

    Time frame: 1 year

    Microbiome based predictions from at least 100 blinded samples will be compared with colonoscopy and pathology results to quantify the sensitivity, specificity and accuracy (reported as %) of the Metabiomics Colon Polyp and Colorectal Cancer Assay for colon polyps. The limited sample size is anticipated to be insufficient to quantify sensitivity to colorectal cancer.

Sponsors and collaborators

Lead sponsor

Metabiomics Corp

Industry

Registry information

Official study title

Metabiomics Neoplasia Clinical Research Study

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
May 20, 2014
Registry last updated
Mar 28, 2017

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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