Austin, TXNCT06620627Now EnrollingIRB Ready

Colorectal Cancer Screening Clinical Trial in Austin, TX

Access cutting-edge colorectal cancer screening treatment through this clinical trial at a research site in Austin. Study-provided care at no cost to qualified participants.

Sponsored by Natera, Inc.

Quick Self-Assessment

See if you qualify for this Austin location

Preparing your pre-screening questions…

Expert Care in Austin

Access colorectal cancer screening specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related colorectal cancer screening treatment provided free

Apply for This Austin Location

Check if you qualify for this colorectal cancer screening clinical trial in Austin, TX

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Austin

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Austin site if eligible
  4. 4Begin participation

About This Colorectal Cancer Screening Study in Austin

The PROCEED-CRC study will prospectively collect blood samples from participants who are at average risk of colorectal cancer (CRC). Samples will be used for research use and the development of a blood-based CRC screening test.

Sponsor: Natera, Inc.

Who Can Participate

Inclusion Criteria

40 years of age or older at time of consent.
Planning or intending to undergo asymptomatic screening colonoscopy.
Able to tolerate venipuncture for research draw(s).
Able and willing to provide blood samples within the 120 days prior to a colonoscopy procedure.
Willing and able to comply with the study visit schedule and study requirements.
Signed informed consent(s) must be obtained prior to participation in the study

Exclusion Criteria

Any prior history of any kind of malignancy (exception: participants who have undergone surgical removal of skin squamous cell or basal cell cancer may be enrolled provided the procedure was completed at least 12 months prior to the date of provision of informed consent for the study)
Had a complete colonoscopy with adequate bowel preparation in the previous nine (9) years.
Undergoing diagnostic colonoscopy for investigation of symptoms such as unexplained and long-lasting diarrhea, overt rectal bleeding, e.g., hematochezia or melena, within the previous 30 days. (Blood on toilet paper, after wiping, does not constitute rectal bleeding)
Undergone colorectal cancer screening within the associated recommended intervals
FOBT/FIT within the previous 12 months
FIT-DNA test within the previous 36 months
Blood-based CRC screening test within the previous 36 months
Computed tomography colonography CTC within the previous 5 years
Flexible sigmoidoscopy within the previous 5 years
Precancerous findings on most recent colonoscopy. This does not include benign, and/or hyperplastic polyps of any size (Note: Tissue biopsies that result in no histopathology findings are acceptable)
Had a prior colorectal resection for any reason other than sigmoid diverticular disease
Diagnosis or personal history of any of the following high-risk conditions for colorectal cancer:
Inflammatory bowel disease (IBD) including chronic ulcerative colitis (CUC) and Crohns disease
Familial adenomatous polyposis (also referred to as FAP, including attenuated FAP)
Hereditary non-polyposis colorectal cancer 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), Gardners Syndrome, Turcots (or Crails) Syndrome, Cowdens Syndrome, Juvenile Polyposis, Cronkhite-Canada Syndrome, Neurofibromatosis and Familial Hyperplastic Polyposis

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Austin?

Yes, this clinical trial (NCT06620627) has an active research site in Austin, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Colorectal Cancer Screening Treatment Options in Austin, TX

If you're searching for colorectal cancer screening treatment options in Austin, TX, this clinical trial (NCT06620627) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Austin research site is actively enrolling participants for this clinical trial. You'll receive care from experienced colorectal cancer screening specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all colorectal cancer screening clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Austin, TX