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Clinical Trials/NCT03891251
NCT03891251RecruitingNot Applicable

Collecting Recorded Videos of Colonoscopy Screening Tests for the Evaluation of the Automatic Polyp Detection System (APDS) Medical Device

Magentiq Eye LTD1 site in 1 country700 target enrollmentStarted: December 19, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
700
Locations
1
Primary Endpoint
Recorded colonoscopy video which was verified by visual inspection to have sufficient high quality.

Study Overview

Brief Summary

The study shall mainly help to better evaluate the performance the APDS device and secondly it may help to assess the potential of the future alpha version of the device to be a useful and effective for the detection of colon Polyps.

Detailed Description

Primary objectives • To evaluate, in objective way, the usability of the future alpha version of the APDS device by testing the sensitivity and specificity of its results achieved from running it on the collected recorded videos of Colonoscopy screening tests of the general population.

Secondary objectives

• When the APDS would be ready for field installation (Beta Version), to install it in the Gastroenterology institute of the medical center, in order to evaluate, as part of a continuation study, the physicians satisfaction from the APDS performance.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Subjects must meet all the - criteria related to regular colonoscopy according to the standard of care at the Gastroenterology Department of the selected center, _In addition the following - criteria have to be met to be eligible for the study:
  • Able to read, understand and provide written Informed Consent;
  • Females or males - older than 18 years old

Exclusion Criteria

  • Any of the following colonoscopy related exclusion criteria will exclude the subject from the study:
  • Bleeding disorder or unacceptable risk of bleeding
  • Terminal illness or life threatening malignancy

Outcomes

Primary Outcomes

Recorded colonoscopy video which was verified by visual inspection to have sufficient high quality.

Time Frame: Half an hour from the end of the procedure at which the video was recorded.

Each recorded video is visually inspected immediately at the end of the procedure by an experienced team member who rates it with a number between 1 (the lowest quality) to 10 (the highest quality). This is a quality scale which indicates the general quality of the recorded video. Only videos with rate above 7 are considered as having sufficient high quality that enables to use them and analyze them.

De-Identified procedure report which was visually inspected to verify that it includes all the needed details about the polyps that were detected during the procedure.

Time Frame: Half an hour from the end of the procedure for which the procedure report was filled-in.

Each de-Identified procedure report is visually inspected immediately at the end of the procedure by an experienced team member who gives it binary score (0 or 1), 1 if it includes all the needed details about the polyps that were detected during the procedure, and 0 if does not include all the needed details about the polyps that were detected during the procedure. Only procedure reports which get the value of 1 can be used for full analysis of the recorded procedure.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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