Lynchburg, VANCT07623902Now EnrollingIRB Ready

CRC Screening Clinical Trial in Lynchburg, VA

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

Sponsored by Jubaan Ltd.

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Expert Care in Lynchburg

Access crc screening specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related crc screening treatment provided free

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Check if you qualify for this crc screening clinical trial in Lynchburg, VA

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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 Lynchburg

    Convenient for VA 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 Lynchburg site if eligible
  4. 4Begin participation

About This CRC Screening Study in Lynchburg

The goal of this clinical trial is to learn if the Gixam device effectively identifies persons with pre-cancer or cancer in the colon and rectum in adults aged 45-84 that are of average risk to develop colorectal cancer and have received a negative result on a Fecal Immunochemical Test (FIT). The main questions it aims to answer are: 1. Is the Gixam Device effective in identifying persons with pre-cancer or cancer in the colon and rectum that have received a negative FIT result? 2. Is the use of the Gixam device safe? Gixam test result will be compared to the findings of a standard of care screening colonoscopy. Study participants will: 1. Undergo the Gixam test 2. Take a FIT at home and ship to a laboratory. 3. Undergo a standard of care screening colonoscopy.

Sponsor: Jubaan Ltd.

Who Can Participate

Inclusion Criteria

Participants aged ≥45 - ≤84 years.
Able to provide a signed informed consent.
Considered by a physician or healthcare provider as being of 'average risk' for CRC.
Scheduled for a screening colonoscopy at investigation site.

Exclusion Criteria

Undergoing colonoscopy for investigation of symptoms.
Has undergone colonoscopy within preceding nine (9) years except for a failed colonoscopy due to poor bowel preparation. Failed colonoscopy must have been within the past year and without therapeutic intervention.
Positive FIT or Fecal Occult Blood Test (FOBT) result within the preceding eleven (11) months.
Has completed Cologuard, Sheild, ColoSense or Epi proColon testing within the preceding three (3) years.
History of colorectal cancer.
Family history of colorectal cancer, defined as having one or more first- degree relatives (parent, sibling, or child) with CRC at any age.
Participant has a diagnosis or medical / family history of any of the following conditions, including:
Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP and Gardner's syndrome)
Hereditary non-polyposis CRC syndrome (also referred to as "HNPCC" or "Lynch Syndrome")
Other hereditary cancer syndromes including but not limited to Peutz-Jeghers Syndrome, MYH-Associated Polyposis (MAP), Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Neurofibromatosis, or Familial Hyperplastic Polyposis.
Participant has a diagnosis or personal history of inflammatory bowel disease (IBD) including chronic ulcerative colitis and/or Crohn's disease.
Participants with a disability to extend their tongue.
Participants with tongue tremor.
Participants with tongue piercing.
Participants that had a dental visit in the 7 days prior to the Gixam test.
Participants that have taken antibiotics or anti-fungal medications in the 14 days prior to the Gixam test.
Participants that have taken anti-inflammatories or probiotics in the 14 days prior to the Gixam test.
Participant is pregnant.
Participant has any condition that in the opinion of the Investigator should preclude participation in the study.

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 Lynchburg?

Yes, this clinical trial (NCT07623902) has an active research site in Lynchburg, VA 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.

CRC Screening Treatment Options in Lynchburg, VA

If you're searching for crc screening treatment options in Lynchburg, VA, this clinical trial (NCT07623902) 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 Lynchburg research site is actively enrolling participants for this clinical trial. You'll receive care from experienced crc 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 crc screening clinical trials near you to find additional studies recruiting in your area.

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