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Trial registered on ANZCTR


Registration number
ACTRN12622000866707
Ethics application status
Approved
Date submitted
7/05/2022
Date registered
17/06/2022
Date last updated
3/11/2024
Date data sharing statement initially provided
17/06/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
Does Artificial Intelligence Improve Polyp Detection at Colonoscopy?
Scientific title
A randomised controlled trial to determine the impact of an artificial intelligence platform on adenoma detection rate during colonoscopy in adults
Secondary ID [1] 307073 0
Nil known
Universal Trial Number (UTN)
U1111-1278-0636
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Colonic Polyps 326230 0
Condition category
Condition code
Oral and Gastrointestinal 323532 323532 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Cancer 323745 323745 0 0
Bowel - Back passage (rectum) or large bowel (colon)

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Usual standard of care from the endoscopist doctor, with addition of Endo-AID (Olympus Corporation) AI module to be on during withdrawal phase of colonoscopy.

-Usual standard of care: single colonoscopy, which may take between 3-30 minutes. During withdrawal phase, which may take between 6 and 60 minutes, the AI module will be activated. It is not known if use of this module will increase the withdrawal time (compared to standard of care, without it).
-The nurses will advise the doctor of the randomisation (AI or standard of care), and turn on the AI device once withdrawal has commenced.
-The AI will analyse the video output from the scope to automatically detect suspected polyps in real-time during withdrawal. Polyps would then be further analysed and resected as per usual standard of care.
Intervention code [1] 323527 0
Diagnosis / Prognosis
Comparator / control treatment
Usual standard of care - colonoscopy withdrawal using doctor preference for polyp detection. This can take between 6-60 minutes. The artificial intelligence module will not be used to examine images taken during this procedure for the control participants.
Control group
Active

Outcomes
Primary outcome [1] 331290 0
ADR (Adenoma Detection Rate) - proportion of patients with at least one histologically proven adenoma or carcinoma. Histology will be assessed using standard procedure in the laboratory.
This data will be gathered from colonoscopy reports and lab reports of patients
Timepoint [1] 331290 0
At time of colonoscopy
Secondary outcome [1] 409435 0
PDR (Polyp Detection Rate): proportion of patients with at least one histologically proven polyp removed. This data will be gathered from colonoscopy reports and lab reports of patients.
Timepoint [1] 409435 0
At time of colonoscopy
Secondary outcome [2] 409436 0
Proximal ADR: proportion of patients with at least one histologically proven polyp removed proximal to the splenic flexture. This data will be gathered from colonoscopy reports and lab reports of patients.
Timepoint [2] 409436 0
At time of colonoscopy
Secondary outcome [3] 409437 0
Mean number of adenomas per colonoscopy (APC) - total number of adenomas divided by the number of colonoscopies performed. This will be comparing standard colonoscopy to AI assisted detection on colonoscopy.
This data will be gathered from colonoscopy reports and lab reports.
Timepoint [3] 409437 0
At time of colonsocopy
Secondary outcome [4] 409438 0
Sessile serrated detection rate (SSL): proportion of patients with at least one histologically proven sessile serrated lesion removed. This data will be gathered from colonoscopy reports and lab reports of patients.
Timepoint [4] 409438 0
At time of colonoscopy
Secondary outcome [5] 409439 0
Non-neoplastic resection rate – proportion of patients with polyps removed that are not histologically proven adenomas, SSLs, or colorectal cancers. This data will be gathered from colonoscopy reports and lab reports of patients.
Timepoint [5] 409439 0
At time of colonoscopy
Secondary outcome [6] 409440 0
Withdrawal time. This will be calculated using a timer (initiated by nursing staff) from the end of the colon (caecum) to withdrawal of the scope from the anus.
Timepoint [6] 409440 0
At time of colonoscopy (at the end)

Eligibility
Key inclusion criteria
• Aged 18 years old or above;
• They require elective colonoscopy for colorectal cancer screening, surveillance, or investigation of symptoms
• Written informed consent obtained.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
• Contraindication or conditions precluding polyp resection (e.g. active gastrointestinal bleeding, significant bleeding tendency, uninterrupted anticoagulation)
• Scheduled staged procedure for polypectomy or biopsy
• Inflammatory Bowel Disease
• Previous bowel resection
• Unable to obtain informed consent

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
prior to colonoscopy initiation, an opaque envelope will be opened by nursing staff with instructions for use of AI or not. Envelopes will be created with instructions by an administrator not participating in study and shuffled.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Participants will be allocated to the two intervention groups at a 1:1 ratio, and the computer-generated randomisation schedule will be pre-determined prior to participant recruitment.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
A sample size of 390 patients per arm is required based on the expected ADR of 35% for both arms, a non-inferiority margin of 10%, power of 90% and an alpha level of 5% (onesided).

Statistical analysis to be performed using IBM SPSS Statistics version 26.0 (New York, USA). Univariate inter-group comparisons performed using the unpaired t-test, where normal distribution had been confirmed by Shapiro-Wilk testing (p>0.05). Non-normally distributed data analysed using the Mann-Whitney U test, and categorical data using the chi-squared or Fisher’s exact test. Preliminary univariate logistic or Poisson regression analysis used to identify potential confounding factors for outcome measures. The association between artificial intelligence use and outcome measures then assessed using multivariable logistic or Poisson regression, incorporating relevant variables with a univariate association threshold of p<0.15. The number of variables used in the multivariable regression analysis approximately limited to the number of adverse events divided by 10, to avoid overfitting. All tests were two-tailed, and p<0.05 was considered statistically significant.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
4/07/2022
Actual
16/03/2023
Date of last participant enrolment
Anticipated
22/12/2023
Actual
11/10/2023
Date of last data collection
Anticipated
22/12/2023
Actual
11/10/2023
Sample size
Target
780
Accrual to date
Final
794
Recruitment outside Australia
Country [1] 24753 0
New Zealand
State/province [1] 24753 0

Funding & Sponsors
Funding source category [1] 311384 0
Commercial sector/Industry
Name [1] 311384 0
Olympus
Country [1] 311384 0
New Zealand
Primary sponsor type
Hospital
Name
Waitakere Hospital
Address
55-75 Lincoln Road, Henderson, Auckland 0610
Country
New Zealand
Secondary sponsor category [1] 312775 0
None
Name [1] 312775 0
Address [1] 312775 0
Country [1] 312775 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 310868 0
Northern B Health and Disability Ethics Committee
Ethics committee address [1] 310868 0
Ethics committee country [1] 310868 0
New Zealand
Date submitted for ethics approval [1] 310868 0
12/12/2021
Approval date [1] 310868 0
03/05/2022
Ethics approval number [1] 310868 0
Project ID: 11946

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 119158 0
Dr Cameron Schauer
Address 119158 0
C/O Gastroenterology Department, Waitakere Hospital
55-75 Lincoln Road, Henderson, Auckland 0610
Country 119158 0
New Zealand
Phone 119158 0
+64210368637
Fax 119158 0
Email 119158 0
cameron.schauer@gmail.com
Contact person for public queries
Name 119159 0
Cameron Schauer
Address 119159 0
C/O Gastroenterology Department, Waitakere Hospital
55-75 Lincoln Road, Henderson, Auckland 0610
Country 119159 0
New Zealand
Phone 119159 0
+64210368637
Fax 119159 0
Email 119159 0
cameron.schauer@gmail.com
Contact person for scientific queries
Name 119160 0
Cameron Schauer
Address 119160 0
C/O Gastroenterology Department, Waitakere Hospital
55-75 Lincoln Road, Henderson, Auckland 0610
Country 119160 0
New Zealand
Phone 119160 0
+64210368637
Fax 119160 0
Email 119160 0
cameron.schauer@gmail.com

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
All data is de-identified once collected (see attached data management plan).

De-identified, raw, line-by-line data for each participant will NOT be made available.


What supporting documents are/will be available?




Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.