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Adenoma Detection Rate in Artificial Intelligence-assisted Colonoscopy

Primary Purpose

Colorectal Cancer, Colorectal Adenoma, Colorectal Neoplasms

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
AI-assisted colonoscopy
Sponsored by
Ismail Gögenur
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colorectal Cancer focused on measuring Artificial intelligence-assisted colonoscopy, Computer-aided polyp detection, Colorectal adenoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Referred for screening colonoscopy due to a positive faecal immunochemical test (FIT) or for Diagnostic colonoscopy due to symptoms/signs or Post-polypectomy surveillance colonoscopy (only patients who had all detected polyps removed in the previous colonoscopy) Exclusion Criteria: Referral for removal of previous detected polyps Emergency colonoscopy Control colonoscopy due to inflammatory bowel disease (IBD)

Sites / Locations

  • Holbæk HospitalRecruiting
  • Zealand University HospitalRecruiting
  • Nykøbing Falster County HospitalRecruiting
  • Næstved HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control

AI-assisted colonoscopy

Arm Description

Conventional colonoscopy, without AI-assistance.

AI-assisted colonoscopy (AIC) using a computer-aided polyp detection and characterization (CADe and CADx) system.

Outcomes

Primary Outcome Measures

Adenoma detection rate (ADR)
ADR = (number of examinations with adenomas/total number of examinations) × 100.

Secondary Outcome Measures

Polyp detection rate (PDR)
PDR = (number of examinations with polyps/total number of examinations) × 100.
Adenomas per colonoscopy (APC)
Number of adenomas found per procedure
Polyps per colonoscopy (PPC)
Number of polyps found during per procedure
Duration of the procedure
Duration of the colonoscopy
Non-neoplastic resection rate (NNRR)
Number of resected non-neoplastic polyps/total number of resected polyps
ADR in the CRC-screening population
Adenoma detection rate (ADR) in one of the patient subgroups
Polyps per positive patient (PPP)
Positive patient = patient with detected polyps during the colonoscopy

Full Information

First Posted
February 3, 2023
Last Updated
February 21, 2023
Sponsor
Ismail Gögenur
Collaborators
Nykøbing Falster County Hospital, Naestved Hospital, Holbaek Sygehus, Slagelse Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05740137
Brief Title
Adenoma Detection Rate in Artificial Intelligence-assisted Colonoscopy
Official Title
Adenoma Detection Rate in Artificial Intelligence-assisted Colonoscopy Performed by Endoscopists With Different Levels of Experience - A Cluster Randomized Controlled Multicenter Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2022 (Actual)
Primary Completion Date
March 3, 2023 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ismail Gögenur
Collaborators
Nykøbing Falster County Hospital, Naestved Hospital, Holbaek Sygehus, Slagelse Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this cluster randomized multicenter controlled clinical trial (RCT) is to investigate whether a combined real time computer-aided polyp detection (CADe) and computer-aided polyp characterization (CADx) system (GI Genius, Medtronic) can increase the adenoma detection rate (ADR) and reduce the performance variability among endoscopists. Participants will be randomized (1:1) to either receive an AI-assisted colonoscopy (AIC) or a conventional colonoscopy (CC). If there is a comparison group: Researchers will compare the AIC-group and the CC-group to see if AIC can increase the ADR significantly.
Detailed Description
Colorectal cancer (CRC) is the third most common cancer, and the second most common cause of cancer-related death worldwide. CRC screening is used for detection and removal of precancerous lesions before they develop into cancer. Colonoscopy is regarded being superior to other screening tests, and is therefore used as the golden standard. Screening colonoscopy is associated with a reduced risk of CRC-related death. Since it is not possible for an endoscopist to determine the histopathology of the polyp with certainty during a colonoscopy, detected pre-malignant lesions should be removed and sent for histological examination. Multiple studies have shown that there is a strong association between findings at the baseline screening colonoscopy and rate of serious lesions at the follow up colonoscopy. Risk factors for adenoma, advanced adenoma and cancer at follow-up colonoscopy are multiplicity, size, villousness, and high degree dysplasia of the adenomas at the baseline screening colonoscopy. The adenoma detection rate (ADR) is the percentage of examinations performed by one endoscopist, in which one or more adenomas are found. This is widely accepted as the main quality indicator for each endoscopist and colonoscopy. There is strong evidence that the ADR is inversely correlated to the incidence of interval CRC. With each 1,0% increase in the ADR there is a 3,0% decrease in the risk of developing CRC. Unfortunately, adenomas and advanced adenomas are frequently missed, and the ADR varies widely among different endoscopists. Also, the quality changes throughout the day. Both the withdrawal time and the ADR decreases by the end of the day, approximately by 20% and 7% respectively. Small improvements in the colonoscopy quality may have great importance for the outcome when screening for CRC. Artificial intelligence (AI) can reduce the performance variability by working as a pair of additional virtual eyes, compensating for perceptual errors due to fatigue, distraction and inaccurate human vision. Within the last few years there have been published several randomized controlled trials (RCT) investigating the efficacy of real time computer-aided detection. Among these, all of the RCT´s which have ADR as the primary outcome, have shown that the use of AI contributes to a significantly higher ADR, compared colonoscopies without assistance of an AI system. Repici et al. have shown that experience of the endoscopist only plays a minor role as a determining factor. Correspondingly, results from a previous study by Liu et al. indicates that CADe systems are not only useful for endoscopists with a low detection rate, but can also increase the ADR for more experienced endoscopists. Kamba et. al reports a significant lower adenoma miss rate (AMR) for CADe-assisted colonoscopy, compared to a conventional colonoscopy. This is independent on the endoscopist´s level of expertise. Other studies conclude that AI probably will benefit the less experienced endoscopists more. However, there are only a limited number of studies investigating the impact of AI when used by less experienced endoscopists. According to a recent RCT from Wallace et al. the use of AI can reduce the AMR by approximately 50%, but primarily due to increased detection of small (<10 mm) flat neoplasia. This difference is slightly higher than in a previous study, in which the relative reduction was approximately 35%. However, in this study there were no significant difference in missed diminutive polyps (<10 mm). In a systematic review the overall withdrawal time was shown to be higher with AI-assisted colonoscopy (AIC), compared to conventional colonoscopy (CC), but the ADR and PDR was also higher. Naturally, there have been concerns about prolonged colonoscopy time, and increased workload if implementing the AI system, since the increased detection of small polyps may lead to unnecessary polypectomy. However, two recent RCT´s report that the unnecessary resection of non-neoplastic polyps did not increase by using the CADe system. The results so far are promising, suggesting that AIC is superior to CC when it comes to polyp and adenoma detection. Routine use of computer-aided polyp detection (CADe) systems could further reduce the incidence of interval CRC, but more clinical data from large multicenter randomized trials are required to understand the actual impact of AI in the daily clinical setting. We have designed a quality assurance multicenter RCT to investigate the effect of real time AI-assistance (GI Genius, Medtronic) on adenoma detection rate (ADR) in both experienced and less experienced endoscopists. We want to investigate whether the CADe system can reduce the performance variability and increase the ADR significantly. The overall aim of this research is to investigate if AI-assistance in colonoscopy can increase the ADR. This prospective, multicenter, randomized controlled trial (RCT) will take place at four endoscopy units in Region Zealand, Denmark. These units are located at Zealand University Hospital (Køge), Nykøbing Falster Hospital, Holbæk Hospital and Næstved Hospital. All units except Næstved Hospital are participating in the national CRC-screening programme. We will screen all patients scheduled for screening, diagnostic, and surveillance colonoscopy. The eligible patients will receive a colonoscopy from an expert or a non-expert endoscopist based on the normal distribution of endoscopists at the endoscopic units.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Colorectal Adenoma, Colorectal Neoplasms
Keywords
Artificial intelligence-assisted colonoscopy, Computer-aided polyp detection, Colorectal adenoma

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A cluster randomized controlled multicenter study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
800 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Conventional colonoscopy, without AI-assistance.
Arm Title
AI-assisted colonoscopy
Arm Type
Active Comparator
Arm Description
AI-assisted colonoscopy (AIC) using a computer-aided polyp detection and characterization (CADe and CADx) system.
Intervention Type
Device
Intervention Name(s)
AI-assisted colonoscopy
Intervention Description
The patients in the intervention group will receive an AI-assisted colonoscopy (AIC) using the computer-aided polyp detection and characterization (CADe and CADx) GI Genius (Medtronic).
Primary Outcome Measure Information:
Title
Adenoma detection rate (ADR)
Description
ADR = (number of examinations with adenomas/total number of examinations) × 100.
Time Frame
5 Months
Secondary Outcome Measure Information:
Title
Polyp detection rate (PDR)
Description
PDR = (number of examinations with polyps/total number of examinations) × 100.
Time Frame
5 Months
Title
Adenomas per colonoscopy (APC)
Description
Number of adenomas found per procedure
Time Frame
5 Months
Title
Polyps per colonoscopy (PPC)
Description
Number of polyps found during per procedure
Time Frame
5 Months
Title
Duration of the procedure
Description
Duration of the colonoscopy
Time Frame
5 Months
Title
Non-neoplastic resection rate (NNRR)
Description
Number of resected non-neoplastic polyps/total number of resected polyps
Time Frame
5 Months
Title
ADR in the CRC-screening population
Description
Adenoma detection rate (ADR) in one of the patient subgroups
Time Frame
5 Months
Title
Polyps per positive patient (PPP)
Description
Positive patient = patient with detected polyps during the colonoscopy
Time Frame
5 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Referred for screening colonoscopy due to a positive faecal immunochemical test (FIT) or for Diagnostic colonoscopy due to symptoms/signs or Post-polypectomy surveillance colonoscopy (only patients who had all detected polyps removed in the previous colonoscopy) Exclusion Criteria: Referral for removal of previous detected polyps Emergency colonoscopy Control colonoscopy due to inflammatory bowel disease (IBD)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ronja Lagström, MD
Phone
+4526800970
Email
rlag@regionsjaelland.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Mustafa Bulut, MD
Email
mub@regionsjaelland.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronja Lagström, MD
Organizational Affiliation
Zealand University Hospital, Køge
Official's Role
Principal Investigator
Facility Information:
Facility Name
Holbæk Hospital
City
Holbæk
ZIP/Postal Code
4300
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julia Agata Bielik, MD
Email
jbie@regionsjaelland.dk
Facility Name
Zealand University Hospital
City
Køge
ZIP/Postal Code
4600
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ronja Lagström, MD
Email
rlag@regionsjaelland.dk
First Name & Middle Initial & Last Name & Degree
Mustafa Bulut, MD
Facility Name
Nykøbing Falster County Hospital
City
Nykøbing Falster
ZIP/Postal Code
4800
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreea-Raluca Diac, MD
Email
anddi@regionsjaelland.dk
Facility Name
Næstved Hospital
City
Næstved
ZIP/Postal Code
4700
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie Gräs Crone, Nurse
Email
jug@regionsjaelland.dk

12. IPD Sharing Statement

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Adenoma Detection Rate in Artificial Intelligence-assisted Colonoscopy

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