A Randomised Paired Design Study of Texture and Colour Enhancement Imaging (TXI) Versus High-definition White Light Endoscopy
- Sponsor
- London North West Healthcare NHS Trust
- Study ID
- NCT07271264
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 16 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- TXI — DIAGNOSTIC_TESTParticipants allocated to the "TXI" group undergo withdrawal using Texture and Colour Enhancement Imaging, while those in the "white light" group receive withdrawal with with high-definition white light endoscopy. Both procedures follow standardized protocols outlined in the study design.
Study Details
Texture and Colour Enhancement Imaging (TXI) improves texture, brightness, and colour in white-light endoscopy to highlight subtle tissue differences. Now available through the EVIS X1 system, early evidence suggests potential value in IBD. Studies show that TXI may help predict ulcerative colitis relapse and performs comparably to dye chromoendoscopy in detecting lesions, though no randomised data exist for dysplasia detection in IBD surveillance. We therefore propose a randomised paired study comparing TXI with high-definition white-light endoscopy for dysplasia detection in IBD surveillance.
Key Dates
- Start date
- Dec 8, 2025
- Status verified
- Apr 2026
- Primary completion
- Dec 8, 2028
- Completion
- Mar 30, 2029
Study Design
- Enrollment
- 219 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- DIAGNOSTIC
Arms
- Active Comparator: TXIParticipants allocated to the "TXI" group undergo withdrawal using Texture and Colour Enhancement Imaging
- Other: White lightParticipants allocated in the "White light " group receive withdrawal with White light
Primary Outcome Measure
To compare the proportion of patients with at least 1 dysplastic lesion detected using TXI compared with high-definition white light endoscopy. [ Time Frame: 6 months ]
Central Contacts
- Jonathan Landy, Consultant Gastroenterologist020 8869 544
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