RECRUITING

Evaluation of the Natera Colorectal Cancer Screening Test in an Average Risk Population (FIND-CRC)

Description

The FIND-CRC study is a prospective collection of samples and data from participants who are at average risk of developing colorectal cancer (CRC). Collected samples and data will be analyzed to evaluate the clinical performance of the Natera CRC Screening Test.

Conditions

Colo-rectal Cancer
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Related Conditions:

Colo-rectal Cancer

Study Overview

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Study Details

Study overview

The FIND-CRC study is a prospective collection of samples and data from participants who are at average risk of developing colorectal cancer (CRC). Collected samples and data will be analyzed to evaluate the clinical performance of the Natera CRC Screening Test.

Evaluation of the Natera Colorectal Cancer Screening Test in an Average Risk Population (FIND-CRC)

Evaluation of the Natera Colorectal Cancer Screening Test in an Average Risk Population (FIND-CRC)

Condition
Colo-rectal Cancer
Intervention / Treatment

-

Contacts and Locations

Austin

Natera, Inc, Austin, Texas, United States, 78753

Austin

Natera, Inc, Austin, Texas, United States, 78753

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Signed informed consent.
  • 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.
  • 1. Any prior history of any kind of malignancy (exception: participants who have undergone surgical removal of skin squamous cell or basal cell cancers may be enrolled, provided the procedure was completed at least 12 months prior to consent for the study).
  • 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:

Ages Eligible for Study

40 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Natera, Inc.,

Study Record Dates

2033-09-30