Follow Up of acuTe Heart failUre: a pRospective Echocardiographic and Clinical Study (FUTURE)
FUTURE-HIT
1 other identifier
observational
998
11 countries
29
Brief Summary
Acute heart failure (AHF) is defined as rapid onset or rapid worsening of typical signs and symptoms of heart failure (HF) according to the 2016 European Society of Cardiology Guidelines. AHF is the first cause of hospitalization in people over 65 in Western countries, accounting for more than 1 million hospitalizations per year in the USA. This disease has many repercussions not only in terms of mortality and morbidity, but also in terms of resources and infrastructures necessary for these patients' treatment, which constitutes a high economic burden for the national health care system. Even with growing knowledge and means, nowadays, the prognosis of AHF is still poor and there are no proven therapies that lead to long-term benefits in terms of reduced mortality. A better management of the acute phase of decompensation, including the definition of effective diagnostic-therapeutic workup and the use of innovative drugs, could improve the course of the disease, with positive effects on the patient (gain in survival and reduction of admissions), but also on the community (containment of the overall health costs). In recent years, numerous scores have been outlined in various AHF settings, considering only a small number of parameters. Several prognostic models have been developed suggesting how difficult it is to evaluate the AHF patients' prognosis. All this effort towards the development of so numerous prognostic models is justified by the fact that, despite the evolution of treatments, the risk of re-hospitalization and of both intrahospital mortality and after discharge remains high. Several studies have investigated potential prognostic factors that could help evaluating the risk of cardiovascular events, but now there is no accurate and complete prognostic score, particularly for AHF patients. Therefore, to date there are no accurate scores or determinants of short- and medium-term prognosis that allow to improve the management of these patients. This will be an observational, prospective, multicentric, international, non-commercial (non-profit) study. The primary endpoint will be to evaluate the best parameters, among clinical, laboratory and echocardiographic variables assessed within 24 hours from the hospital admission and before discharge, that are able to predict rehospitalization for HF and cardiovascular death at 3 and 6 months, in patients admitted to the cardiology department for acute exacerbation of chronic HF or de novo AHF.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2020
Typical duration for all trials
29 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2020
CompletedFirst Submitted
Initial submission to the registry
January 10, 2022
CompletedFirst Posted
Study publicly available on registry
January 24, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2022
CompletedAugust 30, 2022
August 1, 2022
1.9 years
January 10, 2022
August 24, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
predictors of rehospitalization for heart failure and cardiovascular death
The primary endpoint of the FUTURE HIT study will be to evaluate the best parameters, among clinical, labora-tory and echocardiographic variables assessed within 24 hours from the hospital admission and before discharge, that are able to predict rehospitalization for HF and cardiovascular death at 3 and 6 months, in patients admitted to the cardiology department for acute exacerbation of CHF or de novo AHF.
3 and 6 months post discharge
Secondary Outcomes (3)
combined prognostic score of rehospitalization for heart failure and cardiovascular death
3 and 6 months post discharge
Event analysis according to heart failure's different classes (HFpEF, HFmrEF, HFrEF)
3 and 6 months post discharge
Event analysis according to genres
3 and 6 months post discharge
Interventions
LV dimensions, LV mass and indices of LV function LA area and volume Indices of diastolic function (E/A ratio, E/e' ratio) Heart valve assessment according to GL RV dimensions and indices of RV function PAPs (RV-RA gradient and vena cava dimensions and collapsibility) B-lines at lung ultrasounds (comet lung score) Speckle Tracking analysis of LV (GLS), LA (PALS) and RV (LS of free wall) Optional 3D analysis of left and right ventricle
Eligibility Criteria
The FUTURE study population will prospectively recruit patients who will be admitted to a Coronary Intensive Care Unit or a cardiologic ward for AHF (including both acute exacerbation of chronic heart failure and first episode - de novo; the two populations will be also separately analysed). Patients will be recruited at various centres around the world with no restrictions on ethnicity, etiology, LVEF value at the time of admission, and concomitant drug therapies. They will be selected exclusively on the basis of the authorization obtained through the signing of the informed consent and the presence of a good acoustic echocardiographic window.
You may qualify if:
- age ≥18 years
- admission to the cardiology departments for acute heart failure (de novo or exacerbation of chronic heart fail-ure) according to the clinical and instrumental criteria in the current ESC guidelines
- signing of the informed consent
You may not qualify if:
- age \< 18 years
- valve prosthesis
- previous heart transplant or LVAD
- poor acoustic window.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (31)
Blacktown Hospital, Faculty of Medicine, University of Sydney
Sydney, Australia
Department of Cardiology, Antwerp University Hospital
Edegem, Belgium
Hygeia Hospital
Athens, Greece
Laiko General Hospital
Athens, Greece
Red Cross Hospital
Athens, Greece
General Hospital of Elefsina Thriassio
Elefsina, Greece
Onassis Cardiac Surgery center
Kallithea, Greece
Tzaneion General Hospital
Piraeus, Greece
1st Cardiology Department, AHEPA University Hospital
Thessaloniki, Greece
Hippokrateion University Hospital, Medical School, Aristotle University of Thessaloniki, Third Cardiology Department
Thessaloniki, Greece
Centro Cardiologico Monzino IRCCS, Department of Cardiovascular Imaging
Milan, Italy
Division of Cardiology, Nephro-Cardiovascular Department, "S. Agostino- Estense" Public Hospital, University of Modena and Reggio Emilia
Modena, Italy
Division of Cardiology, A.O.R.N. "Sant'Anna e San Sebastiano", Caserta; Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli"
Napoli, Italy
Federico II" University Hospital
Napoli, Italy
Dipartimento Toraco-Cardio-Vascolare, AOU Maggiore della CaritĂ , UniversitĂ del Piemonte Orientale
Novara, Italy
Cardiology Unit, Department of Excellence of Sciences for Health Promotion and Mothernal-Child Care, Internal Medicine and Specialities (ProMISE), University of Palermo, University Hospital Paolo Giaccone
Palermo, Italy
UnitĂ Operativa di Cardiologia, Ospedale Guglielmo da Saliceto
Piacenza, Italy
Division of Cardiology; Department of Surgical, Medical and Molecular Pathology and Critical Care Medicine, AOUP
Pisa, Italy
Fondazione Toscana G. Monasterio
Pisa, Italy
Division of Cardiology - Nocera Inferiore Hospital and L. Vanvitelli University
Salerno, Italy
Heart Department, AOU S. Giovanni e Ruggi, Salerno, Italy.
Salerno, Italy
Department of Medical Biotechnologies Division of Cardiology University of Siena
Siena, Italy
National Institute of Cardiology of Mexico Ignacio ChĂ¡vez
Mexico City, Mexico
Department of Cardiology, Amsterdam University Medical Center
Amsterdam, Netherlands
University Clinic- Department of Cardiology, St Cyril and Methodius University, R. of North Macedonia
Skopje, North Macedonia
Centro Hospitalar UniversitĂ¡rio de SĂ£o JoĂ£o
Porto, Portugal
Emergency Central Militar Hospital
Bucharest, Romania
Hospital Vall d'Hebron
Barcelona, Spain
Department of Cardiology, FSI Hospital
La Marsa, Tunisia
Gazi University
Ankara, Turkey (TĂ¼rkiye)
Dr Siyami Ersek Cardiothoracic Surgery Center
Istanbul, Turkey (TĂ¼rkiye)
Related Publications (40)
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PMID: 20620859BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Matteo Cameli, Prof
Department of Medical Biotechnologies Division of Cardiology University of Siena
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 10, 2022
First Posted
January 24, 2022
Study Start
September 1, 2020
Primary Completion
July 31, 2022
Study Completion
November 30, 2022
Last Updated
August 30, 2022
Record last verified: 2022-08