Congestive Heart Failure Clinical Trial
Official title:
Prospective Study of Heart Failure With Preserved Left Ventricular Ejection Fraction: Prevalence, Characterisation and Prognostic Significance of Cardiac Desynchrony
The purpose of this study is to examine electrical and echocardiographic characteristics and prognosis of consecutive patients admitted with acute heart failure and diagnosed to have heart failure with preserved ejection fraction (HFPEF).
- Time 0: Patients will be screened at the time of presentation to the hospital at
participating centres
- Usually patients will be hospitalised for an acute dyspnea in relation with a pulmonary
congestion. This congestion does not necessarily justify a hospitalization and for part
of the patients a consultation and a dedicated treatment would be good enough to cure
the symptoms.
- Thus, patients seen in emergency for a congestion and diagnosed or known to have a
preserved left ventricular ejection fraction (LV EF > 45%) will be proposed to
participate to the study.
- Patients meeting inclusion criteria will be invited back to the clinic in stable
condition, approximately 4-8 weeks after the initial hospitalization.
- Time 4-8 weeks after initial hospitalisation (NOT after discharge): Comprehensive
history-taking and examinations.
- Any information necessary for the study will be collected by the principal investigator
in each participating center in a dedicated, secure, e-CRF. The access to the e-CRF will
be restrictive to the only principal investigator of each center. The lonely other
persons able to take look to the e-CRF are the study monitors.
- Time 6, 12, and 18 months: Follow up by phone call or review of charts or other records
such as death registries. This part of the study will be performed by the CRAs in the
French Society of Cardiology
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