Completed

Investigating Ultrasound Stiffness Imaging for Predicting Outcomes in Crohn's Disease

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What is being collected

Procedure Data

+ procedure Data

Collected from today forward - Prospective
Procedure
Who is being recruted

Digestive System Diseases+3

+ Gastroenteritis

+ Gastrointestinal Diseases

From 18 to 75 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: September 2012
See protocol details

Summary

Principal SponsorUniversity of Michigan
Last updated: July 30, 2015
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2012

Actual date on which the first participant was enrolled.

Modern medical therapy in Crohn's disease, including immunomodulators and biologic compounds, has revolutionized disease treatment. However, a significant portion of individuals will not respond to medications, most often due to the development of intestinal fibrosis. Over the course of Crohn's disease repeated episodes of inflammation and abnormal wound healing lead to progressive intestinal fibrosis, strictures, and bowel obstruction. While inflammatory Crohn's disease often responds to medical therapy, predominantly fibrostenotic intestinal disease is unresponsive and requires surgery. Our inability to accurately distinguish intestinal inflammation from fibrosis frequently leads to empiric trials of steroids and immunosuppressive therapies. This often proves futile, delays inevitable surgery, and unnecessarily exposes the patient to medication-related risks for months and sometimes years. At present there are no available means to distinguish medically responsive inflammatory disease from predominately fibrotic intestinal disease. The unmet need in this field is an accurate diagnostic technology to determine which patients will benefit from anti-inflammatory therapy, and which patients should go directly to surgery. Non-invasive ultrasound stiffness imaging (USI) may be a surrogate marker of underlying bowel wall fibrosis that aids in predicting if Crohn's disease will be responsive to medical therapy. Two USI methods have recently been developed: Ultrasound elasticity imaging (UEI) uses 2D speckle-tracking to measure tissue strain, a surrogate of fibrosis. The second, shear wave imaging (SWI), is a commercially available technology that measures the speed of ultrasonic shear waves through tissue. Shear waves travel more rapidly through stiff tissue. The central hypothesis of this proposal is that ultrasound stiffness imaging (USI) quantitatively distinguishes predominately inflammatory from fibrotic bowel wall thickening, and therefore is predictive of the likelihood of response to medical therapy or the need for surgery. We plan to objectively test our central hypothesis and attain the objective of this application by pursuing the following three specific aims: Specific Aim 1 (SA-1): Determine if USI stiffness measurements of intestinal strictures in Crohn's patients admitted with small bowel obstruction predicts response or failure of medical therapy based on CDAI and objective inflammatory biomarkers during index hospitalization and at 90 day follow-up. Inpatient Inclusion Criteria: Subjects must be 18 years of age or older Previous diagnosis of Crohn's disease with imaging demonstrating involvement of the ileum Hospital admission imaging demonstrating small bowel dilation (to > 3.5 cm) CDAI score of >220. Inpatient Exclusion Criteria: Active Clostridium difficile colitis/enteritis Presence of abdominal enterocutaneous fistulas in the ultrasound path. Prior abdominal hernia repair with mesh placement in the ultrasound path. Specific Aim 2 (SA-2): Determine if USI stiffness measurements of diseased ileum in Crohn's outpatients starting Anti-Tumor Necrosis Factor-Alpha therapy predicts response to medical therapy based on CDAI and objective inflammatory biomarkers. Outpatient Inclusion Criteria Crohn's patients age 18 and over starting anti-TNF therapy CDAI score > 220 to denote clinical disease activity. Outpatient Exclusion Criteria: Active Clostridium difficile colitis/enteritis Presence of abdominal enterocutaneous fistulas in the ultrasound path Prior abdominal hernia repair with mesh placement in the ultrasound path Current use of prednisone or budesonide Changing anti-TNF due to allergy (including a TNF-induced lupus-like arthritis).

Principal SponsorUniversity of Michigan
Last updated: July 30, 2015
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 75 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Digestive System DiseasesGastroenteritisGastrointestinal DiseasesIntestinal DiseasesInflammatory Bowel DiseasesCrohn Disease

Criteria

3 inclusion criteria required to participate
CDAI score > 220

if INPATIENT: admission for small bowel obstruction

if OUTPATIENT: start of anti-tumor necrosis alpha therapy

3 exclusion criteria prevent from participating
Active Clostridium difficile colitis/enteritis

Presence of abdominal enterocutaneous fistulas in the ultrasound path

Prior abdominal hernia repair with mesh placement in the ultrasound path

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University of Michigan Health System

Ann Arbor, United StatesOpen University of Michigan Health System in Google Maps
CompletedOne Study Center