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Clinical Trial Summary

61 subjects (male or female) between the ages of 45 and 75 will undergo colonoscopy. The primary outcome is Cecal Intubation


Clinical Trial Description

This will be a prospective single-center non-blinded clinical investigation. Each subject will undergo a colonoscopy to the cecum with the Aer-O-Scope Colonoscope System. All pathologies found will be removed. No control group is necessary as the main objective is to reach the cecum. Either the cecum is intubated or it is not. This is true for all colonoscopy procedures. Up to the first ten (10) cases for each physician will be system operation training cases. The primary endpoint of cecal intubation was chosen as this measure is the first quality objective when evaluating colonoscopy quality indicators. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03949777
Study type Interventional
Source GI View Ltd.
Contact
Status Completed
Phase N/A
Start date January 6, 2020
Completion date November 14, 2021

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