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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT06266104
Registration number
NCT06266104
Ethics application status
Date submitted
4/02/2024
Date registered
20/02/2024
Titles & IDs
Public title
Image Enhanced Endoscopy IBD
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Scientific title
Image Enhanced Endoscopy Technology to Improve the Detection of Colorectal Dysplasia in Patients With Inflammatory Bowel Disease
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Secondary ID [1]
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Protocol V1.4_04012024
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Inflammatory Bowel Diseases
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Dysplasia
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Surgery - Image Enhanced Endoscopy Filters
Placebo comparator: Dye Spray Chromoendoscopy - Patients undergoing surveillance with dye spray chromoendoscopy
Active comparator: TXI - Patients undergoing surveillance with TXI (Texture and Colour Enhancement Imaging)
Active comparator: LCI - Patients undergoing surveillance with LCI (Linked Colour Imaging )
Treatment: Surgery: Image Enhanced Endoscopy Filters
Patients that undergoing surveillance and consent to be involved in the study will be randomised to undergo surveillance with LCI, TXI or dye-spray chromoendoscopy (methylene blue).
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Intervention code [1]
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Treatment: Surgery
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Dysplasia Detection Rate
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Assessment method [1]
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Overall Dysplasia Detection rate
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Timepoint [1]
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2 years
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Secondary outcome [1]
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Withdrawal times
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Assessment method [1]
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Withdrawal time for procedure
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Timepoint [1]
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2 years
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Secondary outcome [2]
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Characterisation of lesions
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Assessment method [2]
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Accurate characterisation compared to histology
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Timepoint [2]
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2 years
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Eligibility
Key inclusion criteria
* Patients with inflammatory bowel disease aged 18 to 75 years, that meet Australian recommendations to undergo surveillance colonoscopy will be identified and invited participate in the study.
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Minimum age
18
Years
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Maximum age
75
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
* Any active disease
* Inadequate bowel preparation
* Previous surgical resection involving the colon
* History of bowel cancer
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Study design
Purpose of the study
Diagnosis
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
3/04/2024
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/03/2026
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Actual
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Sample size
Target
270
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Royal Perth Hosptial - Perth
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Recruitment postcode(s) [1]
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6000 - Perth
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Funding & Sponsors
Primary sponsor type
Other
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Name
Royal Perth Hospital
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Dye- spray chromoendoscopy remains the recommended gold standard approach for IBD dysplasia surveillance colonoscopy however recently published European and American guidelines recommend either dye-spray or virtual chromoendoscopy can be used for surveillance. The newer Imaged Enhanced Endoscopy technologies TXI and LCI have not formally been evaluated in IBD surveillance in a randomised controlled trial setting. These modes can easily be applied during colonoscopy and if demonstrated to be effective may save time and eliminate the need for dye-spray chromoendoscopy in the future.
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Trial website
https://clinicaltrials.gov/study/NCT06266104
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Sherman Picardo, MBBS (hon), MSc
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Address
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Country
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Phone
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0892242244
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT06266104