Evaluation of the Natera Colorectal Cancer Screening Test in an Average Risk Population (FIND-CRC)
NCT ID: NCT07046585
Last Updated: 2025-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
25000 participants
OBSERVATIONAL
2025-05-30
2033-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Participants at average risk for colorectal cancer
Participants 40 years of age or older at time of consent, planning or intending to undergo asymptomatic screening colonoscopy.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. 40 years of age or older at the time of consent.
3. Planning or intending to undergo a standard of care colonoscopy.
4. Able to tolerate venipuncture for research draw(s).
5. Able and willing to provide blood samples within the 120 days prior to a standard-of-care pre-bowel preparation procedure and colonoscopy procedure.
6. Willing and able to comply with the study visit schedule and study requirements.
Exclusion Criteria
2. Had a complete colonoscopy with adequate bowel preparation in the previous nine (9) years.
3. Undergoing diagnostic colonoscopy for the investigation of symptoms.
4. Up to date with colorectal cancer screening from any non-invasive test.
5. Precancerous findings on most recent colonoscopy.
6. Had a prior colorectal resection for any reason other than sigmoid diverticular disease.
7. Known personal history of any of the following high-risk conditions:
7a. Inflammatory bowel disease. 7b. Known hereditary condition that would increase risk of colorectal cancer (example Lynch Syndrome).
40 Years
ALL
Yes
Sponsors
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Natera, Inc.
INDUSTRY
Responsible Party
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Locations
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Natera, Inc
Austin, Texas, United States
Countries
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Central Contacts
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Other Identifiers
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25-080-ECP
Identifier Type: -
Identifier Source: org_study_id
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