mt-sDNA 2.0 screening test
Diagnostic TestStool samples will be collected by the subject for the mt-sDNA screening test.
NCT Number: NCT04144738
The primary objective of this study is to assess the sensitivity for colorectal cancer (CRC) and specificity of the mt-sDNA 2.0 test.
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Notify Me40 year and older
All sexes
Observational
Parkway Medical Center, Birmingham, Alabama, United States
Subjects 40 years of age and older scheduled for a screening colonoscopy will be enrolled. Subject will complete the mt-sDNA 2.0 test and the commercially available FIT, followed by completion of a screening colonoscopy. The results of the mt-sDNA screening test and FIT will not be provided to investigators for clinical management of the study subject. Personnel performing the colonoscopy and producing the resulting report and personnel performing histopathologial review of reports or tissue (if applicable) will remain blinded to the results of the mt-sDNA 2.0 screening test results.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subjects must meet the following criteria to be eligible for the study:
Exclusion criteria
Stool samples will be collected by the subject for the mt-sDNA screening test.
Stool samples will be collected by the subject for the FIT test.
Subjects will undergo a screening colonoscopy.
Time frame: Through study completion, an average of 180 days
Time frame: Through study completion, an average of 180 days
Time frame: Through study completion, an average of 180 days
Time frame: Through study completion, an average of 180 days
Time frame: Through study completion, an average of 180 days
Time frame: Through study completion, an average of 180 days
Exact Sciences Corporation
Industry
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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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