CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 740 enrolled
Drug / intervention
i-scan +1 moredevice
Likely dose
Not stated in record
Key inclusion· 3
  • ✓Age 50 to 75 years
  • ✓Intact colon and rectum (no prior surgical resection)
  • ✓Willing to provide informed consent
Key exclusion· 7
  • ✕Age less than 50 or greater than 75 years
  • ✕Inflammatory bowel disease
  • ✕Polyposis syndromes
  • ✕Prior surgical resection of any portion of colon or rectum

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02811419
NCT02811419N/ACompleted
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I-scan Versus Standard High-Definition White Light for the Detection of Adenomatous Polyps

University of California, San Francisco·interventional·Posted Jun 23, 2016·Updated May 1, 2019

In Brief

A clinical study evaluating i-scan and standard high-definition white light for Colorectal Adenomatous Polyps. Completed, enrolled 740 participants across 1 site.

Detailed Summary

This study is a randomized controlled trial to determine whether i-scan can improve the detection of conventional adenomas and sessile serrated adenomas/polyps.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsColorectal Adenomatous Polyps
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 23, 2016
Enrollment StartFeb 1, 2017
Primary CompletionDec 31, 2017
Study CompletionJan 31, 2018
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 10.0 years ago

Interventions

i-scandevice

examination will be performed with i-scan digital enhancement

standard high-definition white lightdevice

examination will be performed with high-definition white light