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

Healthy Clinical Trial

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

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05271656
Study type Interventional
Source Check-Cap Ltd.
Contact
Status Terminated
Phase N/A
Start date May 10, 2022
Completion date July 26, 2023
View Details
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