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Virtual chromoendoscopy vs standard dye-based chromoendoscopy in Inflammatory Bowel Disease (IBD) surveillance.

Virtual chromoendoscopy using i-scan Optical Enhancement for detection and assessment of dysplasia in patients with Inflammatory Bowel Disease - A prospective tandem colonoscopy study.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000390381
Enrollment
200
Registered
2017-03-16
Start date
2017-04-17
Completion date
2018-04-13
Last updated
2017-04-03

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

Conditions

None listed

Brief summary

Dysplasia is an important precursor to bowel cancer in IBD, which can be very challenging to detect. Previous studies suggest that dysplasia is detected in approximately 9% of colonoscopies performed for IBD surveillance. Dye-based chromoendoscopy (DBC) which involves spraying the entire colon with contrast materia such as indigo carmine or methylene blue is thought of as the current gold standard for dysplasia detection. However, dye-based chromoendoscopy is expensive, time consuming and difficult to perform, which limits its use as a surveillance test. A routine survey of Australian Gastroenetrologists suggests that more than half did not use the dye-spray technique. Virtual chromoendoscopy with Pentax i-scan Optical Enhancement(OE) uses in-built technology in the endoscope processor with the same principles as dye-based chromoendoscopy to enhance colonic mucosal pit and vessel pattern. We therefore hypothesise that virtual chromoendoscopy is non-inferior to dye spray chromoendoscopy in detecting dysplasia. It will also consume less resources and time. The aim of our study is to compare virtual and dye-based chromoendoscopy in a prospective tandem colonoscopy study. Research design & methods: We plan to conduct a prospective study, enrolling patients with known IBD who are due to have their standard surveillance colonoscopy to look for dysplasia. A tandem colonoscopy model will be used. Enrolled participants will have a colonoscopy using virtual chromoendoscopy with i-scan OE first during insertion and withdrawal. All lesions detected will be removed or biopsied, as appropriate. On completion of withdrawal, a second look will be performed with dye-spraying as is the current clinical practice. This will allow any additional pathology detected to be treated.

Interventions

Virtual chromoendoscopy using Pentax i-scan Optical Enhancement - this is an imaging system used during colonoscopy to assess the bowel where the endoscopist pushes a button on the colonoscope that enhances the image on the screen, highlighting abnormal features in the bowel lining that may otherwise be missed - the intervention will be administered by an experienced Gastroenterologist - the intervention will be administered during colonoscopy - it will be performed on a single occasion - the

Virtual chromoendoscopy using Pentax i-scan Optical Enhancement - this is an imaging system used during colonoscopy to assess the bowel where the endoscopist pushes a button on the colonoscope that enhances the image on the screen, highlighting abnormal features in the bowel lining that may otherwise be missed - the intervention will be administered by an experienced Gastroenterologist - the intervention will be administered during colonoscopy - it will be performed on a single occasion - the anticipated duration is 10-20 minutes - both the test intervention and the control intervention will be performed during the same colonoscopy procedure - it will be performed in a specialist endoscopy unit

Sponsors

Dr Alexander Dorrington
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inflammatory bowel disease - ulcerative colitis of duration greater than 8 years where there is disease extension beyond the splenic flexure - Crohn's colitis of duration > 8 years

Exclusion criteria

Children (age < 18) Pregnant women Those deemed medically unfit to safely undergo a colonoscopy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026