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Combination of Artificial Intelligence and Mucosal Exposure Device to Enhance Colorectal Neoplasia Detection (AIDEN)

Primary Purpose

Adenoma, Colorectal Cancer, Colorectal Neoplasms

Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
ENDOCUFF
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Adenoma

Eligibility Criteria

45 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Aged 45-85 years old;
  2. They require elective colonoscopy for colorectal cancer screening, polyp surveillance, or investigation of symptoms such as anemia or altered bowel habit;
  3. Written informed consent obtained.

Exclusion Criteria:

  1. Contraindication to colonoscopy (e.g. intestinal obstruction or perforation)
  2. Contraindication or conditions precluding polyp resection (e.g. active gastrointestinal bleeding, uninterrupted anticoagulation or dual antiplatelets)
  3. Staged procedure for polypectomy or biopsy of known unresected lesions
  4. Previous surgical resection of colon
  5. Personal history of colorectal cancer
  6. Personal history of familial polyposis syndrome
  7. Personal history of inflammatory bowel disease
  8. Advanced comorbid conditions (defined as American Society of Anesthesiologists grade 4 or above)
  9. Pregnancy
  10. Unable to obtain informed consent

Sites / Locations

  • Prince of Wales HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

ENDOAID

ENDOAID with ENDOCUFF

Arm Description

CADe system will be used during withdrawal phase of colonoscopy.

CADe system and mucosal exposure device (ENDOCUFF) will be used during withdrawal phase of colonoscopy.

Outcomes

Primary Outcome Measures

ADR
adenoma detection rate

Secondary Outcome Measures

ADR for adenomas of different sizes
<5mm, 5-10mm, >10mm
ADR for adenomas of different colonic segments
caecum, ascending colon, hepatic flexure, transverse colon, splenic flexure, descending colon, sigmoid colon, rectum
Mean number of adenomas per colonoscopy
Mean number of adenomas per colonoscopy
Advanced adenoma detection rate
Advanced adenoma detection rate
Sessile serrated lesion (SSL) detection rate
Sessile serrated lesion (SSL) detection rate
Polyp detection rate
Polyp detection rate
Non-neoplastic resection rate
defined as absence of adenoma or SSL or cancer within resected specimen
Caecal intubation time
Caecal intubation time
Withdrawal time
excluding interventions
Total procedural time
Total procedural time
False positive rate
defined as computer artifacts due to colonic mucosal wall or bowel content lasting for >2 seconds

Full Information

First Posted
June 8, 2022
Last Updated
April 10, 2023
Sponsor
Chinese University of Hong Kong
Collaborators
University Hospital Augsburg
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1. Study Identification

Unique Protocol Identification Number
NCT05414448
Brief Title
Combination of Artificial Intelligence and Mucosal Exposure Device to Enhance Colorectal Neoplasia Detection
Acronym
AIDEN
Official Title
Combination of Artificial Intelligence (ENDOAID) and Mucosal Exposure Device (ENDOCUFF) to Enhance Colorectal Neoplasia Detection: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 7, 2023 (Actual)
Primary Completion Date
March 1, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
University Hospital Augsburg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators hypothesize that the combined use of CADe system (ENDOAID) and mucosal exposure device (Endocuff Vision®) would improve the adenoma detection rate when compared to CADe system alone.
Detailed Description
High polyp miss rates were reported in standard colonoscopies. As a result, a significant proportion of interval CRC was attributed to the missed lesions during index colonoscopy. Risk factors of missed lesions included proximal location, serrate or flat morphology, poor bowel preparation, short withdrawal time and endoscopist experience. To overcome this pitfall, various methods were developed to improve adenoma detection rate (ADR), including distal attachment devices. Among the mucosal exposure devices, Endocuff Vision® was shown to be superior than conventional colonoscopies. Recently, artificial intelligence and automatic computer-aided polyp detection (CADe) systems have developed rapidly and revolutionized the medical field. Nevertheless, there was a potential limitation of 'blind spot' if the endoscopist failed to expose the colonic mucosa adequately leading to missed lesions. To date, no available data or ongoing clinical trial was reported regarding the combined use of CADe and mucosal exposure devices. It may enhance the performance of CADe and provide a novel definitive solution to this unaddressed yet important clinical problem. In this prospective parallel randomized controlled trial, we aim to evaluate the impact of combined use of a new CADe system (ENDOAID) and mucosal exposure device (Endocuff Vision®) on colorectal neoplasia detection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adenoma, Colorectal Cancer, Colorectal Neoplasms

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
1726 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ENDOAID
Arm Type
No Intervention
Arm Description
CADe system will be used during withdrawal phase of colonoscopy.
Arm Title
ENDOAID with ENDOCUFF
Arm Type
Experimental
Arm Description
CADe system and mucosal exposure device (ENDOCUFF) will be used during withdrawal phase of colonoscopy.
Intervention Type
Device
Intervention Name(s)
ENDOCUFF
Intervention Description
ENDOCUFF mucousal exposure device will be used during withdrawal process of the colonoscopy.
Primary Outcome Measure Information:
Title
ADR
Description
adenoma detection rate
Time Frame
During the colonoscopy
Secondary Outcome Measure Information:
Title
ADR for adenomas of different sizes
Description
<5mm, 5-10mm, >10mm
Time Frame
During the colonoscopy
Title
ADR for adenomas of different colonic segments
Description
caecum, ascending colon, hepatic flexure, transverse colon, splenic flexure, descending colon, sigmoid colon, rectum
Time Frame
During the colonoscopy
Title
Mean number of adenomas per colonoscopy
Description
Mean number of adenomas per colonoscopy
Time Frame
During the colonoscopy
Title
Advanced adenoma detection rate
Description
Advanced adenoma detection rate
Time Frame
During the colonoscopy
Title
Sessile serrated lesion (SSL) detection rate
Description
Sessile serrated lesion (SSL) detection rate
Time Frame
During the colonoscopy
Title
Polyp detection rate
Description
Polyp detection rate
Time Frame
During the colonoscopy
Title
Non-neoplastic resection rate
Description
defined as absence of adenoma or SSL or cancer within resected specimen
Time Frame
During the colonoscopy
Title
Caecal intubation time
Description
Caecal intubation time
Time Frame
During the colonoscopy
Title
Withdrawal time
Description
excluding interventions
Time Frame
During the colonoscopy
Title
Total procedural time
Description
Total procedural time
Time Frame
During the colonoscopy
Title
False positive rate
Description
defined as computer artifacts due to colonic mucosal wall or bowel content lasting for >2 seconds
Time Frame
During the colonoscopy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged 45-85 years old; They require elective colonoscopy for colorectal cancer screening, polyp surveillance, or investigation of symptoms such as anemia or altered bowel habit; Written informed consent obtained. Exclusion Criteria: Contraindication to colonoscopy (e.g. intestinal obstruction or perforation) Contraindication or conditions precluding polyp resection (e.g. active gastrointestinal bleeding, uninterrupted anticoagulation or dual antiplatelets) Staged procedure for polypectomy or biopsy of known unresected lesions Previous surgical resection of colon Personal history of colorectal cancer Personal history of familial polyposis syndrome Personal history of inflammatory bowel disease Advanced comorbid conditions (defined as American Society of Anesthesiologists grade 4 or above) Pregnancy Unable to obtain informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Felix Sia
Phone
26370428
Email
felixsia@cuhk.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Lam
Phone
26370428
Email
thomaslam@cuhk.edu.hk
Facility Information:
Facility Name
Prince of Wales Hospital
City
Shatin
State/Province
Hong Kong Island
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felix Sia
Phone
26370428
Email
felixsia@cuhk.edu.hk

12. IPD Sharing Statement

Plan to Share IPD
No

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Combination of Artificial Intelligence and Mucosal Exposure Device to Enhance Colorectal Neoplasia Detection

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