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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03372512
Other study ID # BCM-CMR-T1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 8, 2018
Est. completion date December 15, 2020

Study information

Verified date August 2019
Source Medical University of Vienna
Contact Andreas Kammerlander, MD PhD
Phone 004314040046140
Email andreas.kammerlander@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

It is unclear to what extent systemic fluid overload has an impact on T1-mapping results by cardiovascular mangetic resonance imaging.

In this study, patients will undergo body composition monitoring assessing systemic fluid overload and T1-mapping using MOLLI by cardiovacular magnetic resonance imaging in order to investigate a possible association with each other.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 15, 2020
Est. primary completion date December 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- written informed consent

- patient undergoing cardiovascular magnetic resonance imaging

Exclusion Criteria:

- Unwillingness to participate

- pregnancy

Study Design


Intervention

Diagnostic Test:
Bioimpedance spectroscopy
Fluid overload will be assessed by bioimpedance spectroscopy

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 Native T1-mapping Association of fluid overload and native T1 values of left ventricular myocardium baseline
Primary Extracellular Volume by Cardiovascular magnetic resonance imaging Association of fluid overload and extracellular volume of left ventricular myocardium baseline
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