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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03405987
Other study ID # T1-strain-2436
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2012
Est. completion date December 1, 2020

Study information

Verified date March 2020
Source Medical University of Vienna
Contact Andreas Kammerlander, MD
Phone 014040046140
Email andreas.kammerlander@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The association of T1-mapping (both native and ECV) and strain analysis of LV and RV by CMR will be assessed. Results from strain analysis will be investigated in terms of their prognostic value.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- undergoing CMR

- willingness to participate

Exclusion Criteria:

- <18 years old

- pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Strain analysis by CMR
Strain analysis by CMR will be performed

Locations

Country Name City State
Austria Medical University of 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 Association of native LV T1-values and strain analysis Association of native LV T1-values and strain analysis by CMR Baseline
Primary Association of ECV and strain analysis Association of ECV and strain analysis by CMR Baseline
Primary Association of strain analysis and outcome Association of strain analysis by CMR and outcome (combination of cardiovascular hospitalization or death) 2 years
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