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Assessment of Disease Activity in Ulcerative Colitis by Endoscopic Ultrasound

Assessment of Disease Activity in Ulcerative Colitis by Endoscopic Ultrasound

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01852760
Enrollment
60
Registered
2013-05-14
Start date
2013-09-30
Completion date
2015-07-31
Last updated
2015-10-02

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

Conditions

Inflammatory Bowel Disease, Ulcerative Colitis

Keywords

endoscopic ultrasound, ulcerative colitis, inflammatory bowel disease

Brief summary

In this cross-sectional study patients with active or quiescent ulcerative colitis will be studied to determine the utility of endoscopic ultrasound measurements of rectal wall blood flow and thickness as reliable indices of disease severity and the degree of correlation that exists with validated clinical, endoscopic, and histological indices.

Detailed description

Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) of unknown etiology characterized by diffuse mucosal inflammation limited to the colon. The basis of medical treatment is with agents that reduce the inflammatory process. Tailoring appropriate therapy will depend on disease severity, which can be difficult to identify. A response to therapy may also require months to determine. Medications for induction of remission and/or for maintenance in patients with mild to severe UC include 5-aminosalicylates (5'ASA), corticosteroids, azathioprine (AZA), cyclosporine, and infliximab (IFX). All medications have their own inherent side effect profile. Cost can be a major issue with some medications such as IFX, which can be tens of thousands of dollars annually. Medical management can still fail in those with severe disease necessitating surgical management with a colectomy. Identification of high-risk patients who are candidates for more intensive therapy early in the disease course might be a strategy to improve treatment outcomes and limit cost. This notion of individualizing therapy is attractive and a distinct departure from the current step-care paradigm in which treatments are added sequentially on the basis of symptom-defined treatment failure. However, for this paradigm to be implementable an objective means of accurately stratifying risk must be identified and validated. Accordingly, increased interest has evolved in the use of biomarkers as prognostic tools. Although fecal calprotectin and serum CRP are potential candidates for this role, these tests have limitations. Transabdominal ultrasound (US) has been used in the diagnostic workup of IBD. US was a good surrogate of disease activity when compared to colonoscopy, but is unable to reliably assess the rectal wall which tends to cause the most symptoms in UC. Endoscopic ultrasound (EUS) is a highly accurate diagnostic modality for the assessment of rectal pathology. However, the role of EUS in IBD is not well defined. Tsuga et al showed total wall thickness to be highly predictive for acute inflammation in patients with UC compared to healthy controls and that the degree of rectal wall involvement correlated with endoscopic severity. Higaki et al showed patients with quiescent UC who relapsed had initial sonographic evidence of deep disease activity shown by significantly greater baseline thickness of the first 3 layers of the rectal wall. Yoshizawa et al subsequently demonstrated that inflammation reaching the muscularis propria or deeper predicted the need for colectomy. Hurlstone et al correlated EUS scores with histopathology, endoscopic, and clinical scores and found good concordance to only exist with superficial EUS scores. In all of these studies the investigators who performed the EUS analysis did so with knowledge of the endoscopy scores. This questions the validity of these results due to the potential for bias. Another parameter that shows promise for evaluation of inflammatory burden is EUS evaluation of blood flow. Surprisingly, Doppler flow has not been used to assess bowel wall vascularity in UC with EUS. We believe that assessment of vascularity has the potential to differentiate with a high degree of accuracy active from quiescent disease. Although the existing literature indicates that EUS has potential as an evaluative and prognostic tool the investigators believe that a great deal of additional research is needed to further develop this technology. This study will correlate Doppler EUS and other EUS indices with validated clinical, endoscopic, and histological indices of UC inflammation to assess its utility as a diagnostic tool. It will assess the reproducibility of these indices by calculating inter and intra-observer agreement by blinded expert reviewers. This information may have prognostic importance and might ultimately be used to guide therapy in individual patients.

Interventions

None listed

Sponsors

University of Western Ontario, Canada
CollaboratorOTHER
University of Calgary
CollaboratorOTHER
University of Toronto
CollaboratorOTHER
Dalhousie University
CollaboratorOTHER
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients with a confirmed diagnosis of ulcerative colitis aged 18-85 * Patients termed either active or inactive UC * Patients may be treatment naïve (ie: new diagnosis) or on existing therapy including 5'ASA (oral or topical), AZA, corticosteroids, or IFX

Exclusion criteria

* Inability to or unwillingness to undergo flexible sigmoidoscopy or colonoscopy * Inability to provide informed consent * Crohn's disease 4. Presence of an ileoanal pouch

Design outcomes

Primary

MeasureTime frameDescription
The correlation between EUS indices, clinical, endoscopic, and histological scores of inflammation in UC1 dayThe correlation between EUS indices, clinical, endoscopic, and histological scores of inflammation in UC

Secondary

MeasureTime frameDescription
Interobserver variability of endoscopic and histologic scores1 dayThe agreement by raters of endoscopic and histologic scores of inflammation in UC using the intra-rater and inter-rater reliability.
Interobserver variability of EUS Indices1 dayThe agreement by rater's of EUS indices of inflammation using the intra-rater and inter-rater reliability.
Hyperemia score correlation with UC disease activity1 dayHyperemia on Doppler EUS to assess inflammatory changes in UC patients with active inflammation compared to quiescent disease

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026