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Image Enhanced Endoscopy IBD

Image Enhanced Endoscopy Technology to Improve the Detection of Colorectal Dysplasia in Patients With Inflammatory Bowel Disease

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06266104
Enrollment
270
Registered
2024-02-20
Start date
2024-04-03
Completion date
2026-03-01
Last updated
2024-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysplasia, Inflammatory Bowel Diseases

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.

Interventions

PROCEDUREImage 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).

Sponsors

Royal Perth Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

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.

Exclusion criteria

* Any active disease * Inadequate bowel preparation * Previous surgical resection involving the colon * History of bowel cancer

Design outcomes

Primary

MeasureTime frameDescription
Dysplasia Detection Rate2 yearsOverall Dysplasia Detection rate

Secondary

MeasureTime frameDescription
Withdrawal times2 yearsWithdrawal time for procedure
Characterisation of lesions2 yearsAccurate characterisation compared to histology

Countries

Australia

Contacts

Primary ContactSherman Picardo, MBBS (hon), MSc
sherman.picardo@health.wa.gov.au0892242244

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026