Utilization of NBi in Assessing Luminal INflammaion in IBD (UNBLIND)
Utility of Narrow Band Endoscopy in Predicting Short and Long Term Risk of Relapse in Patients With Quiescent Ulcerative Colitis
1 other identifier
interventional
N/A
1 country
1
Brief Summary
Ulcerative colitis (UC) is a chronic inflammatory condition of unknown aetiology, characterized by a diffuse confluent mucosal inflammation of the colon starting from the rectum with a relapsing and remitting course. Conventional endoscopy was thought to be a reliable parameter of disease activity, but microscopic inflammation can persist despite normal mucosal findings. Histologically detectable inflammation is associated with a greater risk of subsequent relapse. A flare in UC activity is difficult to predict, but a simple, easily measured biological marker of relapse would be important in guiding the most appropriate therapy. Recent technological advances in fiber optics, light sources, detectors, and molecular biology have stimulated development of numerous optical methods that promise to significantly improve our ability to evaluate human epithelium in vivo. These methods, collectively termed "optical biopsy," are nondestructive in situ assays of mucosal histopathology using light that can provide instantaneous tissue assessment. Narrow band imaging (NBI) is a novel technique that enhances the diagnostic capability of endoscopes in characterising tissues by using filters in a redgreenblue (RGB) sequential illumination system. This results in improved mucosal contrast and detail. UC always involves the distal colon and activity is usually greatest in rectosigmoid area. This makes evaluation of the rectum and sigmoid an attractive marker in patients with UC. Unlike serum and faecal markers, endoscopic assessment of the mucosa is unlikely to be affected by systemic disease and would be acceptable test for patients and physicians. We plan to evaluate THE rectosigmoid mucosa in patients with UC by flexible endoscope using both white light and NBI endoscopy. These patients will be followed by for one year or until they relapse, whichever comes first. The aim of our study is to develop endoscopic biomarkers to predict relapse in acute and quiescent UC.
Trial Health
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2013
CompletedFirst Submitted
Initial submission to the registry
January 20, 2014
CompletedFirst Posted
Study publicly available on registry
January 30, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2015
CompletedFebruary 19, 2016
February 1, 2016
2 years
January 20, 2014
February 18, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
Narrow band imaging (NBI)
up to 2 years
Study Arms (1)
NBI
EXPERIMENTALInterventions
Eligibility Criteria
You may qualify if:
- Adult patients referred for lower gastrointestinal endoscopy procedure will be recruited.
- Any age (1885 years), gender or ethnic background
- Able and willing to give an informed consent
You may not qualify if:
- Patients known to be intolerant to endoscopy.
- Patients with severe lifethreatening comorbidity as judged by the investigator.
- Patients on therapy with anticoagulation that may preclude taking any biopsies
- Pregnant women or breast feeding mothers
- Patient with toxic megacolon
- patients on medications known to cause bowel inflammation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Leeds Teaching Hospital NHS Trust
Leeds, LS9 7TF, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 20, 2014
First Posted
January 30, 2014
Study Start
April 1, 2013
Primary Completion
April 1, 2015
Last Updated
February 19, 2016
Record last verified: 2016-02