A Study To Validate An Optimized Multi-Target Stool DNA (Mt-sDNA 2.0) Test For Colorectal Cancer Screening

Overview

About this study

The primary purpose of this study is to assess the sensitivity for colorectal cancer (CRC) and specificity of the mt-sDNA 2.0 test.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Subject is ≥ 40 years of age at the time of enrollment. 
  • Subject presents for a screening colonoscopy per standard of care. 
  • Subject has no symptoms or signs that require immediate, or near term, referral for diagnostic or therapeutic colonoscopy. 
  • Subject is able and willing to sign informed consent.

Exclusion Criteria: 

  • Subject has a history of CRC or advanced precancerous lesions. 
  • Subject has a diagnosis or medical history of any of the following conditions, including:
    • Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP and Gardner's syndrome);
    • Hereditary non-polyposis CRC syndrome (also referred to as "HNPCC" or "Lynch Syndrome");
    • Other hereditary cancer syndromes including but are not limited to Peutz-Jeghers Syndrome, MYH-Associated Polyposis (MAP), Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Neurofibromatosis, or Familial Hyperplastic Polyposis.
  • Subject has a diagnosis or personal history of inflammatory bowel disease (IBD) including chronic ulcerative colitis and/or Crohn's disease. 
  • Subject has a diagnosis of Cronkhite-Canada Syndrome. 
  • Subject has had a positive Cologuard, or fecal occult blood test or FIT within the previous two (2) years. 
  • Subject has undergone a colonoscopy within the previous 9 years. 
  • Subject has had overt rectal bleeding within the previous 30 days. 
  • Subject has any condition that in the opinion of the Investigator should preclude participation in the study.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

John Kisiel, M.D.

Closed for enrollment

Contact information:

Jacquelyn Arndt

5072663966

arndt.jacquelyn@mayo.edu

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Suryakanth Gurudu, M.D.

Closed for enrollment

Contact information:

Brooke Brown

4803014735

brown.brooke@mayo.edu

More information

Publications

Publications are currently not available

Additional contact information

Cancer-related trials contact form

Phone: 855-776-0015 (toll-free)

International patient clinical studies questions