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Comparative Effectiveness of MR Enterography

Primary Purpose

Crohns Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MRE (magnetic resonance enterography)
The Ultrasound scan, (UEI) Ultrasound Elastography Imaging with ARFI (acoustic radiation force impulse)
Study Questionnaires
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Crohns Disease

Eligibility Criteria

1 Month - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pediatric patients under 18 years age.
  • Recently diagnosed with small bowel crohn's disease and have not received any prior treatment for this condition

Exclusion Criteria:

  • Are pregnant.
  • Require sedation to have the MRE exam.
  • Cannot tolerate small enclosed spaces for 60 minutes.
  • Have kidneys that are poorly functioning (eGFR <30ml/min)

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Pediatric Small Bowel Crohn's Disease

Arm Description

MRE (magnetic resonance enterography) performed 4 weeks after SBCD treatment begins, or ends or treatment changes, or at 6 months whichever comes first. One research MRE will be performed and one MRE may or may not be performed as part of your routine care.

Outcomes

Primary Outcome Measures

Effectiveness of MR Enterography, Enteric US, US Elastography Imaging with ARFI
To assess accuracy in imaging techniques

Secondary Outcome Measures

Cost effectiveness and patient imaging preferences
To compare imaging costs and imaging preferences of the patient.

Full Information

First Posted
April 26, 2012
Last Updated
January 20, 2017
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT01593462
Brief Title
Comparative Effectiveness of MR Enterography
Official Title
Comparative Effectiveness of MR Enterography, Enteric Ultrasound, and Ultrasound Elastography Imaging in the Evaluation of Pediatric Small Bowel Crohn Disease
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine the efficacy of ultrasound imaging compared to MRE (Magnetic Resonance Enterography) a form of magnetic resonance imaging (MRI) in accurately diagnosing and following Small Bowel Crohn Disease (SBCD) in children.
Detailed Description
Computed Tomography (CT) is an imaging tool that exposes patients to radiation, and until recently it was the most commonly used imaging method to evaluate small bowel Crohn disease. Recently, Magnetic Resonance Enterography (MRE) which is a form of magnetic resonance imaging that provides detailed images of the bowel and less frequently, Ultrasound (US) are replacing CT as the standard of care imaging tool at some institutions. The investigators would like to determine how effective US imaging is compared to MRI imaging in accurately diagnosing and following SBCD in children. Along with enteric ultrasound (EnUS) we will also be comparing a new ultrasound technology called Ultrasound Elastography Imaging (UEI) for this study in which we will be using a second form of UEI called Acoustic Radiation Force Impulse (ARFI). This technique uses sound waves to asses the stiffness properties of soft tissue. The study will compare costs, patient preferences, and imaging accuracy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohns Disease

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pediatric Small Bowel Crohn's Disease
Arm Type
Experimental
Arm Description
MRE (magnetic resonance enterography) performed 4 weeks after SBCD treatment begins, or ends or treatment changes, or at 6 months whichever comes first. One research MRE will be performed and one MRE may or may not be performed as part of your routine care.
Intervention Type
Procedure
Intervention Name(s)
MRE (magnetic resonance enterography)
Intervention Description
The MRE will take approximately 60 minutes to complete. Enrolled subject will have MRE imaging performed at about 4 weeks after treatment for small bowel crohn's disease begins, and when the treatment ends or changes or at 6 months, whichever comes first. The 4 week MRE will be for research purposes only, the treatment end,change or 6 month MRE may or may not be ordered by the treating physician as part of your routine care. If one is not ordered by the treating physician, the subject will have one performed because of the research study.
Intervention Type
Procedure
Intervention Name(s)
The Ultrasound scan, (UEI) Ultrasound Elastography Imaging with ARFI (acoustic radiation force impulse)
Intervention Description
The US UEI will take about 60 minutes to perform. This exam will be performed by 2 different radiologists and you will have this completed 5 times over the course of the study. This imaging will be performed with the subject drinking oral contrast material. The US, UEI will be completed at baseline, 2 weeks, 4 weeks, 3 months and at treatment end/change or 6 months, whichever comes first.
Intervention Type
Behavioral
Intervention Name(s)
Study Questionnaires
Intervention Description
The subject and their parent will be asked to answer questionnaires 2 weeks after the first MRE and US exams and again after the last imaging examinations are performed at treatment end/change or 6 months, whichever comes first. A Pediatric Crohn Disease Activity Index Assessment will be performed at baseline, 2 weeks, 4 weeks, 3 months, and at treatment end/change or 6 months, whichever comes first. The study questionnaires should take no longer than 10 to 40 minutes to complete.
Primary Outcome Measure Information:
Title
Effectiveness of MR Enterography, Enteric US, US Elastography Imaging with ARFI
Description
To assess accuracy in imaging techniques
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Cost effectiveness and patient imaging preferences
Description
To compare imaging costs and imaging preferences of the patient.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pediatric patients under 18 years age. Recently diagnosed with small bowel crohn's disease and have not received any prior treatment for this condition Exclusion Criteria: Are pregnant. Require sedation to have the MRE exam. Cannot tolerate small enclosed spaces for 60 minutes. Have kidneys that are poorly functioning (eGFR <30ml/min)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Dillman, M.D.
Organizational Affiliation
University of Michigan Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jonathan Dillman, M.D.
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33264183
Citation
Steien DB, Dillman JR, Lopez MJ, Ehrlich P, Adler J. Morphometric Changes in Children With Small Bowel Crohn Disease During Induction of Therapy: A Pilot Study. J Pediatr Gastroenterol Nutr. 2021 Apr 1;72(4):603-609. doi: 10.1097/MPG.0000000000003009.
Results Reference
derived

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Comparative Effectiveness of MR Enterography

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