The CERTAIN Study: Combining Endo-cuff in a Randomized Trial for Artificial Intelligence Navigation
CERTAIN
1 other identifier
observational
1,300
1 country
1
Brief Summary
Colonoscopy is clinically used as the gold standard for detection of colon cancer (CRC) and removal of adenomatous polyps. Despite the success of colonoscopy in reducing cancer-related deaths, there exists a disappointing level of adenomas missed at colonoscopy. "Back-to-back" colonoscopies have indicated significant miss rates of 27% for small adenomas (\< 5 mm) and 6% for adenomas of more than 10 mm in diameter. Studies performing both CT colonography and colonoscopy estimate that the colonoscopy miss rate for polyps over 10 mm in size may be as high as 12%. The clinical importance of missed lesions should be emphasized because these lesions may ultimately progress to CRC. Limitations in human visual perception and other human biases such as fatigue, distraction, level of alertness during examination increases recognition errors and way of mitigating them may be the key to improve polyp detection and further reduction in mortality from CRC. Recent advances in artificial intelligence (AI), deep learning (DL), and computer vision have permitted to develop several AI platforms which have already proved their efficacy in increasing adenoma detection during colonoscopy9,10. As a matter of fact, the improvement in detection due to AI systems is only related to the increased capacity of detecting lesions within the visual field, that is dependent on the amount of mucosa exposed by the endoscopist during the scope withdrawal. Increasing the mucosa exposure would theoretically be a complementary strategy to further improve polyps detection. A number of distal attachments have been tested to increase the mucosal exposure by flattening mucosal folds, including a transparent cap, cuff or rings. The additional diagnostic yield obtained by the second generation of cuff (Endocuff Vision; Olympus America, Center Valley, Pa, USA) was recently investigated by a meta-analysis of randomized controlled trials, showing a significant improvement in adenoma detection rate, and adenomas per colonoscopy, with a reduction in the mean withdrawal time without any increase in adverse events compared with standard high-definition colonoscopy without any distal attachment. In conclusion, technologies providing either mucosal image enhancement (Artificial Intelligence assisted colonoscopy) or mucosal exposure device (Endocuff Vision assisted colonoscopy) significantly improved adenoma detection rate (ADR). However, the diagnostic yield obtained by combining the different strategies is still unknown.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2021
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 15, 2020
CompletedFirst Posted
Study publicly available on registry
December 21, 2020
CompletedStudy Start
First participant enrolled
July 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
May 31, 2022
CompletedSeptember 14, 2022
September 1, 2022
11 months
December 15, 2020
September 13, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Diagnostic yield
To compare the additional diagnostic yield obtained by EndoCuff Vision aided-colonoscopy to the yield obtained by the Standard colonoscopy performed with the Artificial Intelligence ¬-GI GeniusTM- assistance in different colonoscopy settings.
12 Months
Study Arms (2)
AI arm
Standard colonoscopy with Artificial Intelligence-GI GeniusTM
Cuff arm
Endo-cuff Vision aided colonoscopy with Artificial Intelligence -GI GeniusTM
Interventions
Eligibility Criteria
All 40-80 years-old subjects undergoing a colonoscopy for gastrointestinal symptoms, fecal immunohistochemical test positivity, primary screening or post-polypectomy surveillance.
You may qualify if:
- subjects undergoing a colonoscopy for gastrointestinal symptoms, fecal immunohistochemical test positivity, primary screening or post-polypectomy surveillance
You may not qualify if:
- subjects with personal history of CRC, or IBD.
- subjects affected with genetic mutations such as Lynch syndrome or Familiar Adenomatous Polyposis.
- patients with inadequate bowel preparation (defined as Boston Bowel Preparation Scale \> 2 in any colonic segment).
- patients with previous colonic resection.
- patients on antithrombotic therapy, precluding polyp resection.
- patients with history of colonic strictures, precluding ECV use.
- patients who were not able or refused to give informed written consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Endoscopy Unit, Humanitas Research Hospital
Rozzano, Milano, 20089, Italy
Related Publications (1)
Spadaccini M, Hassan C, Rondonotti E, Antonelli G, Andrisani G, Lollo G, Auriemma F, Iacopini F, Facciorusso A, Maselli R, Fugazza A, Bambina Bergna IM, Cereatti F, Mangiavillano B, Radaelli F, Di Matteo F, Gross SA, Sharma P, Mori Y, Bretthauer M, Rex DK, Repici A; CERTAIN Study Group. Combination of Mucosa-Exposure Device and Computer-Aided Detection for Adenoma Detection During Colonoscopy: A Randomized Trial. Gastroenterology. 2023 Jul;165(1):244-251.e3. doi: 10.1053/j.gastro.2023.03.237. Epub 2023 Apr 14.
PMID: 37061169DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 15, 2020
First Posted
December 21, 2020
Study Start
July 1, 2021
Primary Completion
May 31, 2022
Study Completion
May 31, 2022
Last Updated
September 14, 2022
Record last verified: 2022-09
Data Sharing
- IPD Sharing
- Will not share