Boca Raton, FLNCT06880055Now EnrollingIRB Ready

Colo-rectal Cancer Clinical Trial in Boca Raton, FL

Access cutting-edge colo-rectal cancer treatment through this clinical trial at a research site in Boca Raton. Study-provided care at no cost to qualified participants.

Sponsored by Guardant Health, Inc.

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Expert Care in Boca Raton

Access colo-rectal cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related colo-rectal cancer treatment provided free

Apply for This Boca Raton Location

Check if you qualify for this colo-rectal cancer clinical trial in Boca Raton, FL

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

Why Participate?

  • No-Cost Study Care

  • Local to Boca Raton

    Convenient for FL 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 Boca Raton site if eligible
  4. 4Begin participation

About This Colo-rectal Cancer Study in Boca Raton

The Shield post-approval study (PAS) is a prospective, longitudinal study supplemented with Real World Evidence (RWE) to evaluate the longitudinal performance of Shield in an average risk population at a second round of testing for individuals between the ages of 45 and 81 at average risk of CRC using colonoscopy as the reference method.

Sponsor: Guardant Health, Inc.

Who Can Participate

Inclusion Criteria

Subjects aged 45-81 years at time of consent
Intending to undergo a standard of care Shield test
Considered by a physician or healthcare provider as being of 'average risk' for CRC; 'Average-risk' individuals in the context of CRC screening are defined as those who do not have symptoms of CRC and do not have increased risk factors for the disease (i.e., prior diagnosis of CRC, adenomatous polyps, or inflammatory bowel disease; family history of CRC or known hereditary predisposition to CRC).
Subject agrees to comply with study procedures and associated standard of care assessments.

Exclusion Criteria

Undergoing colonoscopy for investigation of symptoms
Personal history of colorectal cancer (CRC), adenomas, or other related cancers
Family history of CRC, defined as having one or more first-degree relative (parent, sibling, or child) diagnosed with CRC at any age
Positive result on another colorectal cancer screening method within the last six months, or:
12 months for fecal occult blood test (FOBT) or fecal immunochemical test (FIT)
36 months for FIT-DNA test
Personal history of any of the following high-risk conditions for colorectal cancer:
Inflammatory Bowel Disease (IBD), including chronic ulcerative colitis (CUC) and Crohn's disease
Familial adenomatous polyposis (FAP)
Other hereditary cancer syndromes including but not limited to:
Hereditary non-polyposis colorectal cancer syndrome (HNPCC) or "Lynch Syndrome", Peutz- Jeghers Syndrome, MUTYH Polyposis (MAP), Gardner's Syndrome, Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Cronkhite-Canada Syndrome, Neurofibromatosis and Familial Hyperplastic Polyposis
Positive Shield test result within the previous 3 years
History of any malignancy (patients who have undergone surgical removal of skin squamous 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)
Known diagnosis of inflammatory bowel disease
Currently taking any anti-neoplastic or disease-modifying anti-rheumatic drugs (DMARDs)
Any major physical trauma (e.g., disruption of tissue, surgery, organ transplant, blood product transfusion) within the 30 days leading up to the provision of informed consent
Known medical condition which, in the opinion of the Investigator, should preclude enrollment into the study
Participation in a clinical research study in which an experimental medication has been administered or may be administered within the 30 days leading up to providing informed consent or may be administered through the time of colonoscopy

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 Boca Raton?

Yes, this clinical trial (NCT06880055) has an active research site in Boca Raton, FL 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.

Colo-rectal Cancer Treatment Options in Boca Raton, FL

If you're searching for colo-rectal cancer treatment options in Boca Raton, FL, this clinical trial (NCT06880055) 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 Boca Raton research site is actively enrolling participants for this clinical trial. You'll receive care from experienced colo-rectal cancer 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 colo-rectal cancer clinical trials near you to find additional studies recruiting in your area.

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