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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04220450
Other study ID # NAFLD-CMR-2436
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date June 15, 2021

Study information

Verified date January 2020
Source Medical University of Vienna
Contact Andreas Kammerlander, MD PhD
Phone 0043 1 40400 46140
Email andreas.kammerlander@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

On clinically indicated Cardiovascular Magnetic Resonance studies, native T1-times and extracellular volume of the liver will be assessed and findings correlated with established risk calculators for non-alcoholic fatty liver disease.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 800
Est. completion date June 15, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers
Gender All
Age group 18 Months and older
Eligibility Inclusion Criteria:

- Referred for Cardiovascular Magnetic Resonance Imaging

Exclusion Criteria:

- Non-compatible Devices

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
T1 mapping on Cardiovascular Magnetic Resonance Studies
On clinically indicated Cardiovascular Magnetic Resonance Imaging Studies, native T1-times and extracellular volume will be determined

Locations

Country Name City State
Austria Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Dr. Andreas Kammerlander

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation NAFLD and liver T1mapping Correlation NAFLD risk score and liver T1-mapping (native and ECV9 cross-sectional within one year
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