A Comparative Study of MRI, US and CE for Assessing Treatment Response in Known Crohn's Disease
Primary Purpose
Crohn Disease
Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Diagnostic work-up
Sponsored by
About this trial
This is an interventional diagnostic trial for Crohn Disease
Eligibility Criteria
Inclusion Criteria:
- An established diagnosis of CD
- Age > 18 years
- Ileocolonoscopy: Endoscopically active CD (SES-CD ≥ 3)
- Clinically active CD (Harvey-Bradshaw Index ≥ 5 or Crohn's Disease Activity Index ≥ 150)
- Clinical indication for medical treatment with corticosteroids or biological therapy
- Signed informed consent
Exclusion Criteria:
- Acute bowel obstruction
- Intake of NSAIDs or acetylsalicylic acid ≤ 4 weeks before inclusion except prophylactic treatment with low dose Aspirin (≤ 150 mg per day)
- Pregnancy or lactation
- Alcohol or drug abuse
- Known gastrointestinal disorder other than inflammatory bowel disease
- Renal failure defined by a plasma-creatinine above the normal reference range
- Claustrophobia, cardiac pacemaker or implanted magnetic foreign bodies that precludes MREC
- Interpreter required or inability to understand the oral and written information
- Bowel surgery performed between pre- and post-treatment assessment
Sites / Locations
- Sygehus LillebaeltRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Diagnosis
Arm Description
Outcomes
Primary Outcome Measures
Diagnostic accuracy
Sensitivity and specificity of SBCCE, MREC and US for the diagnosis of ulcer healing in the terminal ileum and colon
Secondary Outcome Measures
Diagnostic accuracy fCal
Sensitivity and specificity of fecal calprotectin for the diagnosis of ulcer healing in the terminal ileum and colon
Diagnostic accuracy CRP
Sensitivity and specificity of C-reactive protein for the diagnosis of ulcer healing in the terminal ileum and colon
Bowel wall thickening
Changes of bowel wall thickening (mm) assessed with US under medical treatment of Crohn's disease
Elastography
Changes of shear wave elastography (m/s) assessed with US under medical treatment of Crohn's disease
Ultrasound activity index
Changes of Limberg score assessed with US under medical treatment of Crohn's disease
Full Information
NCT ID
NCT03435016
First Posted
February 2, 2018
Last Updated
November 19, 2022
Sponsor
Sygehus Lillebaelt
Collaborators
Odense University Hospital, Hospital of South West Jutland
1. Study Identification
Unique Protocol Identification Number
NCT03435016
Brief Title
A Comparative Study of MRI, US and CE for Assessing Treatment Response in Known Crohn's Disease
Official Title
A Comparative Study of Magnetic Resonance Imaging, Ultrasound and Capsule Endoscopy of the Small and Large Intestine for Assessing Treatment Response in Known Crohn's Disease
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
March 1, 2023 (Anticipated)
Study Completion Date
March 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sygehus Lillebaelt
Collaborators
Odense University Hospital, Hospital of South West Jutland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to evaluate non-invasive imaging techniques for assessing treatment response in known Crohn's disease.
Comparing imaging modalities:
The applicability of small bowel colon capsule endoscopy (SBCCE), magnetic resonance enterocolonography (MREC) and ultrasound (US) for diagnosing ulcer healing after medical treatment in patients with symptomatic Crohn's disease compared to ileocolonoscopy.
Sensitivity and specificity for ulcer healing
Changes in activity parameters for SBCCE, MREC and US before and after medical treatment.
Feasibility of SBCCE, MREC and US for assessing treatment response in known Crohn's disease.
Treatment induced bowel wall alterations visualized with ultrasound:
A non-blinded study of bowel wall changes detected with repeated US examination during medical treatment of known Crohn's disease.
Changes in bowel wall thickness, vascularity and elastography parameters, and time to normalization of the bowel wall.
Detailed Description
The aim of this study is to evaluate the applicability of SBCCE, MREC and US for diagnosing ulcer healing after medical treatment in patients with symptomatic CD compared to the current gold standard (ileocolonoscopy).
This is a prospective, blinded, multicenter study. Patients are recruited from 3 centers in the Region of Southern Denmark managing adult patients with inflammatory bowel diseases. Each patient goes through a standardized work-up including medical history, physical examination, C-reactive protein, fecal calprotectin, ileocolonoscopy, SBCCE, MREC and US before and 10-12 weeks after medical treatment with corticosteroids or biological therapy (Infliximab, Adalimumab, Vedolizumab or Ustekinumab). All examinations are reviewed and described in a standardized fashion. The radiologists and physicians describing SBCCE, MREC, and US are blinded to the findings at ileocolonoscopy and the other imaging modalities. Ileocolonoscopy serves as the diagnostic gold standard, and endoscopic disease activity is assessed with SES-CD.
LOGISTICS: Patients go through an accelerated diagnostic work-up at inclusion and after 10-12 weeks of medical treatment. In patients undergoing their first diagnostic work-up, ileocolonoscopy with biopsies is performed last to avoid false positive lesions at SBCCE. In patients with an established diagnosis, examinations can be performed in a random order provided that tissue samples are not taken during ileocolonoscopy. All diagnostic procedures should be completed within two weeks. If one imaging modality is contraindicated it is classified as "not performed". If ileocolonoscopy (gold standard) is contraindicated, the patient is excluded from the study. All radiological examinations are performed in the Department of Radiology, Lillebaelt Hospital Vejle. Ileocolonoscopy and SBCCE are performed at the local gastroenterology department.
During the pre- and post-treatment assessment, radiological examinations and SBCCE are analyzed by physicians blinded to the result of ileocolonoscopy and the other bowel examinations. However, at the post-treatment assessment, physicians are not blinded to the pre-treatment examinations. After completing all diagnostic procedures, the treating gastroenterologist is provided with the results of SBCCE, MREC and US.
EXTENDED ULTRASOUND STUDY: Patients are scheduled for additional US procedures after 2 and 4 weeks. Procedures are performed without blinding, i.e. the physician is aware of the results of the pre-treatment assessment and the preceding US examinations. If the bowel wall normalizes at week 2, the subsequent procedure is cancelled. Fecal calprotectin is measured before each US procedure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn 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
75 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Diagnosis
Arm Type
Other
Intervention Type
Diagnostic Test
Intervention Name(s)
Diagnostic work-up
Other Intervention Name(s)
Ileocolonoscopy, MR enterocolonography, Ultrasound, Small bowel colon capsule endoscopy
Intervention Description
Patients are examined with all modalities. MR enterocolonography, ultrasound, and small bowel capsule endoscopy are compared against ileocolonoscopy (gold standard).
Primary Outcome Measure Information:
Title
Diagnostic accuracy
Description
Sensitivity and specificity of SBCCE, MREC and US for the diagnosis of ulcer healing in the terminal ileum and colon
Time Frame
8-10 weeks
Secondary Outcome Measure Information:
Title
Diagnostic accuracy fCal
Description
Sensitivity and specificity of fecal calprotectin for the diagnosis of ulcer healing in the terminal ileum and colon
Time Frame
8-10 weeks
Title
Diagnostic accuracy CRP
Description
Sensitivity and specificity of C-reactive protein for the diagnosis of ulcer healing in the terminal ileum and colon
Time Frame
8-10 weeks
Title
Bowel wall thickening
Description
Changes of bowel wall thickening (mm) assessed with US under medical treatment of Crohn's disease
Time Frame
8-10 weeks
Title
Elastography
Description
Changes of shear wave elastography (m/s) assessed with US under medical treatment of Crohn's disease
Time Frame
8-10 weeks
Title
Ultrasound activity index
Description
Changes of Limberg score assessed with US under medical treatment of Crohn's disease
Time Frame
8-10 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
An established diagnosis of CD
Age > 18 years
Ileocolonoscopy: Endoscopically active CD (SES-CD ≥ 3)
Clinically active CD (Harvey-Bradshaw Index ≥ 5 or Crohn's Disease Activity Index ≥ 150)
Clinical indication for medical treatment with corticosteroids or biological therapy
Signed informed consent
Exclusion Criteria:
Acute bowel obstruction
Intake of NSAIDs or acetylsalicylic acid ≤ 4 weeks before inclusion except prophylactic treatment with low dose Aspirin (≤ 150 mg per day)
Pregnancy or lactation
Alcohol or drug abuse
Known gastrointestinal disorder other than inflammatory bowel disease
Renal failure defined by a plasma-creatinine above the normal reference range
Claustrophobia, cardiac pacemaker or implanted magnetic foreign bodies that precludes MREC
Interpreter required or inability to understand the oral and written information
Bowel surgery performed between pre- and post-treatment assessment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael D Jensen, MD, PhD
Phone
0045 7940 6345
Email
michael.dam.jensen@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Mie A Juel, MD
Phone
0045 7940 6345
Email
mie.agerbaek.juel@rsyd.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael D Jensen, MD, PhD
Organizational Affiliation
Lillebaelt Hospital Vejle
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sygehus Lillebaelt
City
Vejle
ZIP/Postal Code
7100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael D Jensen, MD, PhD
Phone
0045 7940 6345
Email
michael.dam.jensen@rsyd.dk
First Name & Middle Initial & Last Name & Degree
Mie A Juel, MD
Phone
0045 7940 6345
Email
mie.agerbaek.juel@rsyd.dk
First Name & Middle Initial & Last Name & Degree
Michael D Jensen, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mie A Juel, MD
First Name & Middle Initial & Last Name & Degree
Jacob B Brodersen, MD
First Name & Middle Initial & Last Name & Degree
Jens Kjeldsen, Professor, PhD
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data will not be available to other researchers.
Learn more about this trial
A Comparative Study of MRI, US and CE for Assessing Treatment Response in Known Crohn's Disease
We'll reach out to this number within 24 hrs