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.
Full Title of Study: “Collecting Recorded Videos of Colonoscopy Screening Tests for the Evaluation of the Automatic Polyp Detection System (APDS) Medical Device”
- Study Type: Observational
- Study Design
- Time Perspective: Prospective
- Study Primary Completion Date: December 2019
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.
• 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.
- Other: Collecting recorded videos of Colonoscopy screening tests
- 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.
Clinical Trial Outcome Measures
- 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.
Participating in This Clinical Trial
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:
1. Able to read, understand and provide written Informed Consent;
2. Females or males – older than 18 years old
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
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
- Lead Sponsor
- Magentiq Eye LTD
- Provider of Information About this Clinical Study
- Overall Official(s)
- Harold Jacob, MD, Principal Investigator, Senior Gastroenterologist
- Overall Contact(s)
- Dror Zur, Ph.D., +972(54)7555922, firstname.lastname@example.org
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