- Trials with a EudraCT protocol (1,476)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
1,476 result(s) found for: Heart Failure.
Displaying page 6 of 74.
EudraCT Number: 2013-001498-25 | Sponsor Protocol Number: CRLX030A2301 | Start Date*: 2013-09-09 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, randomized, double-blind, placebo-controlled phase IIIb study to evaluate the efficacy, safety and tolerability of Serelaxin when added to standard therapy in acute heart failure pa... | ||
Medical condition: Acute heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) BE (Completed) SE (Completed) IE (Completed) BG (Completed) HU (Completed) PT (Completed) LT (Prematurely Ended) IT (Completed) CZ (Completed) AT (Completed) EE (Completed) DK (Completed) ES (Completed) LV (Prematurely Ended) NL (Completed) GR (Completed) GB (Completed) PL (Completed) NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005394-66 | Sponsor Protocol Number: ESR-20-21070 | Start Date*: 2022-02-21 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE | |||||||||||||
Full Title: Effects of Dapagliflozin on cardiac deformation and clinical outcomes in heart failure with reduced and mildly reduced ejection fraction | |||||||||||||
Medical condition: heart failure with left ventricular ejection fraction <50% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002823-16 | Sponsor Protocol Number: 02-2011 | Start Date*: 2011-07-27 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: Effects of Vitamin D in patients affected by heart failure | |||||||||||||
Medical condition: Heart failure is a condition that occurs when the heart loses its normal ability to pump blood to maintain vital body functions and, therefore, works with lower efficiency. Several studies have sho... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001117-13 | Sponsor Protocol Number: C3BS-C-11-01 | Start Date*: 2012-11-14 | |||||||||||
Sponsor Name:Celyad SA | |||||||||||||
Full Title: Efficacy and Safety of Bone Marrow-Derived Mesenchymal Cardiopoietic Cells (C3BS-CQR-1) for the Treatment of Chronic Advanced Ischemic Heart Failure | |||||||||||||
Medical condition: Chronic advanced symptomatic heart failure secondary to ischemic cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) HU (Completed) PL (Completed) SE (Completed) ES (Completed) IE (Completed) BG (Completed) LT (Completed) EE (Prematurely Ended) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013929-42 | Sponsor Protocol Number: 39588146AHF2001 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of JNJ-39588146 in Subjects with Heart Failure | |||||||||||||
Medical condition: JNJ-39588146 is being developed for the treatment of heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005302-26 | Sponsor Protocol Number: DW.0701.005.2020P | Start Date*: 2023-01-05 | |||||||||||
Sponsor Name:John Paul II Hospital | |||||||||||||
Full Title: The effect of sacubitril/valsartan versus ramipril on left ventricular function and remodeling in patients with ischemic heart failure with mid-range ejection fraction | |||||||||||||
Medical condition: heart failure with moderately reduced ejection fraction (HFmrEF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011441-11 | Sponsor Protocol Number: LAICA/09 | Start Date*: 2009-09-21 | |||||||||||
Sponsor Name:Dr. Francisco Marrero Rodríguez. Hospital Universitario de Canarias | |||||||||||||
Full Title: Estudio Randomizado Doble Ciego y Controlado con Placebo Para Evaluar la Eficacia y Seguridad de la Administración Intermitente y a Largo Plazo de Levosimendan en Pacientes con Insuficiencia Cardia... | |||||||||||||
Medical condition: Insuficiencia Cardiaca avanzada | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007407-86 | Sponsor Protocol Number: LevoRep | Start Date*: 2009-09-14 | |||||||||||
Sponsor Name:Medizinische Universität Innsbruck - Universitätsklinik für Innere Medizin III | |||||||||||||
Full Title: Efficacy and safety of pulsed infusions of levosimendan in outpatients with advanced heart failure | |||||||||||||
Medical condition: Chronic heart failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021258-20 | Sponsor Protocol Number: EAST | Start Date*: 2011-06-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Kompetenznetz Vorhofflimmern e.V. (AFNET) | ||||||||||||||||||||||||||||||||||||||
Full Title: Early treatment of Atrial fibrillation for Stroke prevention Trial (EAST) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Atrial fibrillation, stroke, heart failure, myocardial infarction, cognitive dysfunction | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) DK (Completed) NL (Completed) CZ (Completed) BE (Completed) ES (Completed) PL (Completed) IT (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004193-18 | Sponsor Protocol Number: LEVOS-001 | Start Date*: 2017-02-16 |
Sponsor Name:Semmelweis University, Heart and Vascular Center | ||
Full Title: Effect of repetitive levosimendan treatment on clinical outcomes of chronic heart failure patients: focus on optimal patient selection based on novel cardiac biomarkers. | ||
Medical condition: A total of 80 symptomatic patients with severe ischaemic or non-ischaemic cardiomyopathy will be enrolled in the study. Those, who were implanted a device and proved to be non-responders or low res... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003460-13 | Sponsor Protocol Number: GN16CA007 | Start Date*: 2018-02-13 | ||||||||||||||||||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | ||||||||||||||||||||||||||||
Full Title: The effects of sacubitril/valsartan compared to valsartan on left ventricular remodelling in patients with asymptomatic left ventricular systolic dysfunction after myocardial infarction: a randomi... | ||||||||||||||||||||||||||||
Medical condition: Asymptomatic (New York Heart Association ≤2) left ventricular systolic dysfunction (defined as ejection fraction ≤40% measured by Simpson's biplane using transthoracic echocardiography) at least 3... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002914-30 | Sponsor Protocol Number: LCZ696-17 | Start Date*: 2017-11-06 |
Sponsor Name:FIMABIS | ||
Full Title: LCZ696 in heart failure patients with reduced ejection fraction and high comorbidity: effect on left ventricular remodeling and fibrosis assessed by novel heart failure biomarkers and cardiac magne... | ||
Medical condition: Chronic heart failure NYHA class II-IV with reduced ejection fraction (EF =< 40%) and elevated NT-proBNP ≥ 600 pg/mL, but 400 pg/mL if hospitalized for heart failure within 12 months | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005325-10 | Sponsor Protocol Number: DC2008exe001 | Start Date*: 2009-04-08 | ||||||||||||||||
Sponsor Name:VU University Medical Center | ||||||||||||||||||
Full Title: The effect of exenatide compared to insulin glargine on cardiac function and metabolism in type 2 diabetic patients with congestive heart failure (NYHA II): a randomized-controlled trial | ||||||||||||||||||
Medical condition: Cardiac function and metabolism in type 2 diabetic patients with congestive heart failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000972-32 | Sponsor Protocol Number: P-110875-01 | Start Date*: 2011-06-14 | |||||||||||
Sponsor Name:FERRER INTERNACIONAL, S.A | |||||||||||||
Full Title: Estudio randomizado, abierto, con endpoint enmascarado, cruzado, de dosis única para comparar la farmacodinamia de TORASEMIDA- LP 10 mg, TORASEMIDA-LI 10 mg y FUROSEMIDA-LI 40 mg en pacientes con i... | |||||||||||||
Medical condition: INSUFICIENCIA CARDIACA COMPENSADA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004667-13 | Sponsor Protocol Number: N/A | Start Date*: 2018-04-24 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: Effect of Iron (III) Isomaltoside 1000 on Cardiac Energetics in Anaemic and Non-anaemic Patients with Symptomatic Chronic Heart Failure and Iron Deficiency: The Ferric Iron in Heart Failure (FERRIC... | ||||||||||||||||||
Medical condition: Chronic Heart Failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002513-35 | Sponsor Protocol Number: CRLX030A3301 | Start Date*: 2013-11-28 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, prospective, randomized, open label study to assess the effect of serelaxin versus standard of care in acute heart failure (AHF) patients. | ||
Medical condition: Acute heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) BE (Completed) PT (Prematurely Ended) BG (Completed) LT (Completed) PL (Prematurely Ended) LV (Prematurely Ended) EE (Completed) FI (Prematurely Ended) SI (Prematurely Ended) GR (Prematurely Ended) ES (Prematurely Ended) HR (Prematurely Ended) DK (Prematurely Ended) IS (Prematurely Ended) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005767-26 | Sponsor Protocol Number: 2006-KarviD-II | Start Date*: 2007-05-22 | |||||||||||||||||||||
Sponsor Name:The Department of Calcium- and Bone-metabolic Diseases | |||||||||||||||||||||||
Full Title: The effect of calcium and vitamin D on the heartmusclef unction | |||||||||||||||||||||||
Medical condition: Effect of intervention with vitamin D on degree of cardiac incompensation: Degree of cardiac incompensation has been related to vitamin D deficiency and secondary hyperparathyroidism in clinical st... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002396-18 | Sponsor Protocol Number: 2015-602295-02 | Start Date*: 2015-11-30 | |||||||||||
Sponsor Name:Ethicare GmbH | |||||||||||||
Full Title: ORODISPERSIBLE MINITABLETS OF ENALAPRIL IN YOUNG CHILDREN WITH HEART FAILURE DUE TO CONGENITAL HEART DISEASE | |||||||||||||
Medical condition: Heart Failure due to Congenital Heart Disease | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Prematurely Ended) NL (Ongoing) AT (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001637-18 | Sponsor Protocol Number: CKI- 302 | Start Date*: 2006-11-13 | |||||||||||
Sponsor Name:NovaCardia Inc (wholly owned subsidiary of Merck & Co. Inc) | |||||||||||||
Full Title: A multicentre, randomised, double-blind, placebo-controlled study of the effects of KW-3902 Injectable Emulsion on heart failure signs and symptoms and renal function in subjects with acute heart f... | |||||||||||||
Medical condition: Patients being admitted to hospital for acute heart failure (AHFS) with volume overload and renal impairment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) CZ (Completed) BE (Completed) DK (Prematurely Ended) GB (Completed) HU (Completed) DE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001637-10 | Sponsor Protocol Number: 12008 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:HUCH, Division of Cardiology | |||||||||||||
Full Title: Acute heart failure in acute coronary syndrome: Double blind comparison of levosimendan and placebo | |||||||||||||
Medical condition: Acute coronary syndrome treated with percutaneous coronary intervention (PCI) Patients suffering from acute heart failure after the procedure will be randomised to the study | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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