Characterization of Heart Failure With Preserved Ejection Fraction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain

About this trial

The goals of this research will be to define some of the mechanisms underlying the progression and complications of heart failure (HF) with preserved left ventricular ejection fraction (HFPEF)

Aim 1: to evaluate the differences in cardiac structure, function and fibrosis markers through the spectrum of HF stages in order to deepen the understanding of the pathophysiology driving HF progression.

Aim 2: to define the mechanisms by which HF risk factors, such as hypertension, diabetes, obesity, and renal insufficiency, interact with age to increase HF risk, and to evaluate the role of precipitating factors such as myocardial ischemia, atrial fibrillation in HFPEF.

Aim 3: to determine prognostic factors in HFPEF patients, by following these patients over time. Accordingly the investigators will correlate baseline data (echocardiographic, MRI or biomarkers) with incident cardiovascular events and determine whether these measures provide incremental prognostic information beyond clinical characteristics.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • cMR

    Diagnostic test

    cardiac MRI done to complete the diagnosis

  • biomarker

    Biological/Vaccine

    Biomarker correlation with cMR parameters Prognostic information

Treatment groups

500 Participants
are divided into 3 treatment groups
Group A: HFpEFActive comparator 2 interventions
Group B: ControlsActive comparator 2 interventions
Group C: HFrEFActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Prognosis with a follow up including HF hospitalizations and/or deaths.

A follow up will be done by the investigators. After that, they will determine if fibrosis estimated by cMR or biomarkers is a significant prognostic factor.

Time frame
6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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