Evaluation of C-Scan Capsule in Identifying Subjects With Elevated Risk of Colon Polyps

The main objective of the study is to determine the ability of the C-Scan system to identify subjects who are at elevated risk for colon polyps. This will be evaluated by comparing the C-Scan data to colonoscopy data. The C-Scan procedure is therefore performed before the colonoscopy procedure, in order to compare these tests and evaluate the C-Scan system's effectiveness. During the C-scan procedure, Subjects will be asked to come for an appointment in a clinic, during this appointment, the C-Scan Track will be placed on the participant's back. The participant will then be asked to swallow the C-Scan capsule whereafter they are free to continue their routine. Participants will start intake of fiber pills 5 days, and contrast agent 48 hours prior to C-Scan capsule ingestion and will continue intake up to the capsule's natural excretion. A standard colonoscopy procedure will be performed within 60 days following C-Scan Cap ingestion.

The Sponsor and the C-Scan data analysis team shall be blind to subject's optical colonoscopy data until the C-Scan report is created.

All study participants will undergo the C-Scan System procedure, followed by a standard of care optical colonoscopy

Subjects will be provided with contrast agent and dietary fiber pills, and instructed to start intake of fiber pills 5 days, and contrast agent 48 hours prior to scheduled C-Scan capsule ingestion. C-Scan system intervention includes ingestion of the C-Scan Cap and attachment of the C-Scan Track to the subject's lower back. The subject is required to keep the C-Scan Track attached to the lower back and to continue intake of contrast agent and dietary fiber pills until the C-Scan Cap's natural excretion. Standard of care optical colonoscopy will be performed within 60 days from the C-Scan Cap ingestion.

Demonstrate the accuracy of the C-Scan system in identifying subjects with colon polyps comparing to optical colonoscopy (OC).

For each subject the primary efficacy endpoints are dichotomous diagnosis using the C-Scan device (Test) and optical colonoscopy (Reference standard). Reference standard will be considered "positive" ("1") if at least one polyp of at least 6 mm is found. Test will be considered with elevated risk for polyps ("1") if either at least one polyp of at least 6 mm is found or long WGTT* occurred. The above endpoints will be used to calculate sensitivity and specificity examined in the primary analysis. *Long WGTT is defined as more than 73 hours for male and more than 97 hours for female.

Reference standard will be considered "positive" ("1") if at least one polyp of at least 10 mm is found.

Reference standard will be considered "positive" ("1") if at least one polyp of at least 10 mm is found.

Frequency of patients who experienced device or procedure related serious adverse events up to 7±3 days from capsule excretion. In addition, AEs and SAEs will be presented by severity and relation to device and procedure.

Inclusion Criteria: Subjects 45-75 years old Able to provide a signed informed consent. Willing and able to comply with the specified study requirements and can be contacted by telephone. Scheduled for colonoscopy procedure no later than 60 days after C-Scan ingestion Maximal abdominal circumference < 125 cm. Exclusion Criteria: Subject who is not a suitable candidate for a colonoscopy Known history of dysphagia or other swallowing disorders. History of the following: Colorectal polyps A personal history of CRC A family history of CRC or adenomatous polyps diagnosed in a relative before 60 years of age A history of inflammatory bowel disease of significant duration One of two (2) hereditary syndromes Known motility disorders: Chronic Constipation: less than three (3) bowel movements/week, without the use of laxatives within the last 3 months. Ongoing diarrhea defined as passage of loose or watery stools at least three times within 24-hour Delayed gastric emptying. Known IBD (Crohn's, Ulcerative Colitis) Prior history of gastrointestinal tract surgery. Prior history of abdominal surgery that might cause bowel strictures leading to capsule retention, as determined by a physician Any condition believed to have an increased risk for capsule retention, known strictures, known bowel adhesion or 'obstacles' to free passage of the capsule (such as esophageal diverticulosis, intestinal tumors, radiation enteritis) or incomplete colonoscopies as determined by a physician. Significant change in diameter and frequency of stool within the last 3 months. GI bleeding within the last 3 months i.e., rectal outlet bleeding, hematochezia or melena. Implanted cardiac device or any other implanted active device Known sensitivity to iodine Acute kidney failure Known condition which precludes compliance or is contraindicated with study and/or device instructions. Any procedure requiring contrast agent, or which may introduce electronic interference (such as magnetic resonance imaging, DEXA scan) or an imaging procedure pre-scheduled within 14 days of C-Scan ingestion Nuclear imaging procedure within the four (4) weeks preceding the C-Scan procedure. Known condition of opioid use disorder and/or alcoholism. Women who are either pregnant or nursing at the time of screening (to be verified by urine or serum pregnancy test for woman of child- bearing potential who are not post-menopausal or undergone surgical sterilization). Concurrent participation in another clinical trail using any investigational drug or device. Previous colonoscopy performed five (5) years or less before date of enrolment Subjects who tend to hyperhidrosis in the back area