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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05239260
Other study ID # Liver-T1-CMR-2575
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2022
Est. completion date January 1, 2023

Study information

Verified date February 2022
Source Medical University of Vienna
Contact Katharina Mascherbauer
Phone 0043 1 40400 48590
Email katharina.mascherbauer@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Correlation between CMR T1-times, liver T1-times, fibroscan and fluid status to identify the correlation and pathogenesis of liver disease in patients with heart disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date January 1, 2023
Est. primary completion date May 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A 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:
CMR
CMR

Locations

Country Name City State
Austria Medical University Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Impact of fluid status on liver elastography and T1-times 5 months
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