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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05322109
Other study ID # EA2/017/22
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 23, 2021
Est. completion date December 12, 2021

Study information

Verified date April 2022
Source German Heart Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The diagnosis of heart failure with preserved ejection fraction has so far been made primarily according to criteria determined by echocardiography, or invasively by measuring the left ventricular filling pressures. Increasingly, CMR is also evaluated with regard to the diagnosis of cardiac insufficiency with preserved pump function.However, it is still unclear which parameters can be used meaningfully for diagnostics.To answer this question, the investigators want to retrospectively evaluate data collected from patients with a clinical indication for CMR and coronary angiography.


Description:

Heart failure with preserved pump function is a common disease that is associated with a high level of suffering for the patient. The diagnosis has so far been made primarily according to criteria determined by echocardiography, or invasively by measuring the left ventricular filling pressures. With its high spatial resolution and the possibility of tissue-specific diagnostics, cardiac MRI (CMR) offers outstanding possibilities in cardiac imaging without exposing the patient to ionizing radiation. Increasingly, CMR is also evaluated with regard to the diagnosis of cardiac insufficiency with preserved pump function. However, it is still unclear which parameters can be used meaningfully for diagnostics. There is evidence for a correlation with invasively increased LVEDP, although the number of patients examined in the previous studies was still small. In addition, possible influences from medication and clinical parameters were not examined. To answer this question, the investigators want to retrospectively evaluate data collected from patients with a clinical indication. The significance of the study is that in the future CMR could supplement echocardiography in the diagnosis of HFpEF and further reduce the need for invasive diagnostics.


Recruitment information / eligibility

Status Completed
Enrollment 190
Est. completion date December 12, 2021
Est. primary completion date December 12, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with CMR and left heart catheterization including LVEDP measurement within the same month Exclusion Criteria: - Severe Valve Dysfunction or Pericardial/Pleural Disease - Contraindictaion for CR or Cath

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
CMR
Clinically indicated cardiac magnetic resonance tomography executed according to international guideline recommendations.

Locations

Country Name City State
Germany Deutsches Herzzentrum Berlin Berlin

Sponsors (1)

Lead Sponsor Collaborator
German Heart Institute

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Extracellular myocardial volume (%) Estimated percentage of extracellular volume of the myocardium One montth
Primary Left atrial volume (ml) Volume of the left atrium in mililiters One month
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