Diagnostic Potential of PET/MRI in Cardiac Sarcoidosis
Primary Purpose
Sarcoidosis, Cardiomyopathies
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
18F-FDG-PET/MRI
18F-GE180-PET/MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Sarcoidosis focused on measuring Diagnostic Imaging, Positron Emission Tomography Computed Tomography, Magnetic Resonance Imaging
Eligibility Criteria
Inclusion Criteria:
- Heart department: Suspicion of myocardial sarcoidosis after contrast enhanced cardiac MRI
- Lung department: Clinically verified lung and/or mediastinal sarcoidosis
Exclusion Criteria:
- Known malignancies
- Treatment for sarcoidosis started
- Severe arrhythmia
- Patients with pacemakers or defibrillator
- Claustrophobia
- Known alcohol or drug abuse
- Kidney failure (eGFR < 30)
- Weight > 120 kg
- Diabetes Mellitus type I and II
- Patients that take immunosuppressive or immunomodulatory medication for any reason
Sites / Locations
- St Olav University Hospital, Dept Radiology and Nuclear Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
18F-FDG-PET/MRI
18F-GE180-PET/MRI
Arm Description
Outcomes
Primary Outcome Measures
diagnostic accuracy of a combined 18F-FDG and 18F-GE-180 PET/MRI examination for diagnosing cardiac sarcoidosis
Secondary Outcome Measures
Full Information
NCT ID
NCT03561025
First Posted
June 6, 2018
Last Updated
November 16, 2020
Sponsor
St. Olavs Hospital
Collaborators
Norwegian University of Science and Technology, University Hospital, Essen
1. Study Identification
Unique Protocol Identification Number
NCT03561025
Brief Title
Diagnostic Potential of PET/MRI in Cardiac Sarcoidosis
Official Title
Diagnostic Potential of PET/MRI in Cardiac Sarcoidosis: A Pilot Study Combining Advanced MRI and 18F-FDG and 18F-GE180 PET of the Myocardium
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
October 1, 2020 (Actual)
Study Completion Date
October 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Olavs Hospital
Collaborators
Norwegian University of Science and Technology, University Hospital, Essen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the study is to find better and more specific non-invasive methods to diagnose and stage cardiac sarcoidosis with the use of advanced imaging modalities, simultaneous 3T MRI and PET. Cardiac sarcoidosis is a disease of possibly fatal outcome in young people. The use of a combined PET/MRI system with 18F-FDG and a new inflammation-tracer (18F-GE180) can become a future game changer.
Sarcoid induced focal inflammation in myocardium should show high 18F-GE180 uptake. 18F-GE180 PET scans will give reliable data about inflammatory sarcoidosis activity in the myocardium. 18F-GE180 PET is expected to improve diagnostic accuracy compared to 18F-FDG-PET and/or contrast enhanced MRI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoidosis, Cardiomyopathies
Keywords
Diagnostic Imaging, Positron Emission Tomography Computed Tomography, Magnetic Resonance Imaging
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare Provider
Allocation
Non-Randomized
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
18F-FDG-PET/MRI
Arm Type
Active Comparator
Arm Title
18F-GE180-PET/MRI
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
18F-FDG-PET/MRI
Intervention Description
Contrast-enhanced MRI scanning after injection of 18F-FDG
Intervention Type
Diagnostic Test
Intervention Name(s)
18F-GE180-PET/MRI
Intervention Description
Contrast-enhanced MRI scanning after injection of 18F-GE180
Primary Outcome Measure Information:
Title
diagnostic accuracy of a combined 18F-FDG and 18F-GE-180 PET/MRI examination for diagnosing cardiac sarcoidosis
Time Frame
One day after the test
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Heart department: Suspicion of myocardial sarcoidosis after contrast enhanced cardiac MRI
Lung department: Clinically verified lung and/or mediastinal sarcoidosis
Exclusion Criteria:
Known malignancies
Treatment for sarcoidosis started
Severe arrhythmia
Patients with pacemakers or defibrillator
Claustrophobia
Known alcohol or drug abuse
Kidney failure (eGFR < 30)
Weight > 120 kg
Diabetes Mellitus type I and II
Patients that take immunosuppressive or immunomodulatory medication for any reason
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edmund Søvik
Organizational Affiliation
St. Olavs Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
St Olav University Hospital, Dept Radiology and Nuclear Medicine
City
Trondheim
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Diagnostic Potential of PET/MRI in Cardiac Sarcoidosis
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