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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02335801
Other study ID # TOSCA0001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2013
Est. completion date December 1, 2019

Study information

Verified date December 2018
Source Federico II University
Contact Antonio Cittadini, Professor
Phone +39 081 7464375
Email antonio.cittadini@unina.it
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The objective of this study is to determine whether the presence of metabolic alteration and anabolic deficiencies in patients with chronic heart failure are able to identify a subset of patients with poor outcome.


Description:

Despite the effectiveness of the neurohormonal model to explain the progression of heart failure and the many insights that it provided for the development of new therapies, there is increasing clinical evidence that suggests that our current models fail to completely explain the disease progression. Thus, neurohormonal models may be necessary but not sufficient to explain all aspects of disease progression in the failing heart. There is evidence suggesting that in heart failure there is a metabolic imbalance characterized by the predominance of the catabolic status over the anabolic drive.

Aim of this registry is to determine the prevalence of hormone/metabolic deficiencies in heart failure patients and to look for possible association with clinical variables. Moreover, enrolled patients will be followed up for a mean of 2,5 years in order to collect outcome data including all-cause mortality, cardiovascular mortality, hospitalizations.

This is a multi-center observational study involving several Italian Department of Cardiology, Endocrinology, Internal Medicine


Recruitment information / eligibility

Status Recruiting
Enrollment 650
Est. completion date December 1, 2019
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients of either sex affected by CHF, secondary to ischemic or idiopathic dilated cardiomyopathy

- left ventricle ejection fraction 40% or less

Exclusion Criteria:

- severe liver disease

- serum creatinine levels >2.5 mg/dl

- history of active cancer with life expectancy below 1 year

- acute coronary syndrome in the previous 6 months

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Policlinico di Bari Bari
Italy U.O. di Cardiologia 2 IRCCS-Istituto Scientifico di Riabilitazione di Cassano delle Murge Cassano delle Murge Bari
Italy Policlinico "Vittorio Emanuele" University of Catania Catania
Italy Unità Operativa di Malattie Cardiovascolari del Policlinico Mater Domini Catanzaro
Italy UOC di Medicina Interna IRCCS Oasi Maria SS Enna
Italy UOC Clinica Medica Dipartimento ad Attività Integrata di Medicina Azienda Ospedaliera-Universitaria S.Anna Ferrara
Italy University of Florence Florence
Italy IRCCS Policlinico San Donato Milanese Milan
Italy Department of Traslational Sciences - Federico II University Naples
Italy AORN V. Monaldi SUN - Centro di diagnosi e cura Cardiomiopatie e Scompenso Cardiaco Napoli
Italy Dipartimento di Scienze Biomediche Avanzate Università degli studi di Napoli Federico II Napoli
Italy Santa Maria della Pietà Hospital Nola Napoli
Italy U.O.S. Endocrinologia Ospedali Riuniti "Villa Sofia - Cervello" Palermo
Italy U.O. di Riabilitazione Cardiologica IRCCS S. Raffaele Pisana Rome
Italy UOC Endocrinologia e Malattie del Metabolismo Policlinico Universitario Gemelli Rome
Italy U.O. di Cardiologia e UTIC Ospedale S. Maria Incoronata dell'Olmo Salerno
Italy Medicina Generale ad Indirizzo Endocrinologico - d.O. Azienda Ospedaliera Universitaria Integrata Verona

Sponsors (1)

Lead Sponsor Collaborator
Federico II University

Country where clinical trial is conducted

Italy, 

References & Publications (4)

Arcopinto M, Isgaard J, Marra AM, Formisano P, Bossone E, Vriz O, Vigorito C, Saccà L, Douglas PS, Cittadini A. IGF-1 predicts survival in chronic heart failure. Insights from the T.O.S.CA. (Trattamento Ormonale Nello Scompenso CArdiaco) registry. Int J C — View Citation

Bossone E, Limongelli G, Malizia G, Ferrara F, Vriz O, Citro R, Marra AM, Arcopinto M, Bobbio E, Sirico D, Caliendo L, Ballotta A, D'Andrea A, Frigiola A, Isgaard J, Saccà L, Antonio C; T.O.S.CA. Investigators. The T.O.S.CA. Project: research, education a — View Citation

Cittadini A, Marra AM, Arcopinto M, Bobbio E, Salzano A, Sirico D, Napoli R, Colao A, Longobardi S, Baliga RR, Bossone E, Saccà L. Growth hormone replacement delays the progression of chronic heart failure combined with growth hormone deficiency: an exten — View Citation

Cittadini A, Saldamarco L, Marra AM, Arcopinto M, Carlomagno G, Imbriaco M, Del Forno D, Vigorito C, Merola B, Oliviero U, Fazio S, Saccà L. Growth hormone deficiency in patients with chronic heart failure and beneficial effects of its correction. J Clin Endocrinol Metab. 2009 Sep;94(9):3329-36. doi: 10.1210/jc.2009-0533. Epub 2009 Jul 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other reduction in peak oxygen consumption outcome assessed during scheduled visits every six months (up to 5 years)
Other left ventricular volumes outcome assessed during scheduled visits every six months (up to 5 years)
Primary all-cause mortality and hospitalization outcome assessed during scheduled visits or phone calls every six months (up to 5 years)
Secondary cardiovascular mortality outcome assessed during scheduled visits or phone calls every six months (up to 5 years)
Secondary cardiovascular hospitalizations outcome assessed during scheduled visits or phone calls every six months (up to 5 years)
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