- Trials with a EudraCT protocol (211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
211 result(s) found for: Systolic dysfunction.
Displaying page 1 of 11.
EudraCT Number: 2009-011006-42 | Sponsor Protocol Number: vs.3.23-02-2009 | Start Date*: 2009-07-13 | ||||||||||||||||
Sponsor Name:Rigshospitalet, Hjertemedicinsk afd. B | ||||||||||||||||||
Full Title: Sildenafil and diastolic dysfunction after AMI | ||||||||||||||||||
Medical condition: Diastolic dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001150-88 | Sponsor Protocol Number: MEN/03/ZOF-CHF/001 | Start Date*: 2005-05-06 | |||||||||||
Sponsor Name:Menarini International Operation Luxembourg -SA | |||||||||||||
Full Title: Comparison between zofenopril and ramipril in combination with ASA on the extent of cardiovascular risk in patients with systolic left ventricular dysfunction after acute myocardial infarction (SMI... | |||||||||||||
Medical condition: Systolic left ventricular dysfunction after AMI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002020-25 | Sponsor Protocol Number: 052017 | Start Date*: 2018-08-31 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: ANGIOTENSIN–NEPRILYSIN INHIBITION IN DIASTOLIC DYSFUNCTION AFTER AMI | |||||||||||||
Medical condition: Diastolic dysfunction after acute myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011559-38 | Sponsor Protocol Number: CL2-44121-004 | Start Date*: 2010-03-16 | ||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
Full Title: Evaluation of the effects of 4 oral dosages of S 44121 versus placebo on cardiac function and NT-proBNP in patients with chronic heart failure and left ventricular dysfunction not treated with a be... | ||||||||||||||||||
Medical condition: Chronic heart failure and left ventricular dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) ES (Completed) IT (Completed) GB (Completed) LV (Completed) EE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000896-99 | Sponsor Protocol Number: AC16148 | Start Date*: 2017-06-20 | ||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
Full Title: A multicentre prospective randomised open-label blinded end-point controlled trial of high-sensitivity cardiac troponin I-guided combination angiotensin receptor blockade and beta blocker therapy t... | ||||||||||||||||||
Medical condition: Myocardial toxicity and the development of left ventricular systolic dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003905-25 | Sponsor Protocol Number: HAC2018-001 | Start Date*: 2019-06-27 | |||||||||||
Sponsor Name:H.A.C. Pharma | |||||||||||||
Full Title: Evaluation of efficacy and tolerance of fludrocortisone (Flucortac) in the treatment of neurogenic orthostatic hypotension | |||||||||||||
Medical condition: Neurogenic Orthostatic Hypotension (NOH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014940-12 | Sponsor Protocol Number: CL2-44121-006 | Start Date*: 2010-03-11 | |||||||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
Full Title: Evaluation of the anti-arrhythmic effects of 3 oral dosages of S 44121 versus placebo in patients with chronic heart failure and left ventricular systolic dysfunction at risk for ventricular arrhyt... | |||||||||||||||||||||||
Medical condition: Chronic Heart Failure and left ventricular systolic dysfunction at risk for ventricular arrhythmia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) HU (Completed) SK (Completed) ES (Completed) PT (Completed) GB (Completed) CZ (Completed) DE (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011558-16 | Sponsor Protocol Number: CL2-44121-003 | Start Date*: 2010-03-16 | ||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
Full Title: Evaluation of the effects of 4 oral dosages of S 44121 versus placebo on cardiac function and NT-proBNP in patients with chronic heart failure and left ventricular dysfunction. A 12-week, randomize... | ||||||||||||||||||
Medical condition: Chronic heart failure and left ventricular dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) ES (Completed) IT (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005278-59 | Sponsor Protocol Number: 20050222 | Start Date*: 2006-12-22 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Assess the Efficacy and Safety of Darbepoetin Alfa Treatment on Mortality and Morbidity in Heart Failure (HF) Subjects with Symp... | |||||||||||||
Medical condition: Heart Failure Subjects with Symptomatic Left Ventricular Systolic Dysfunction and Anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) LT (Completed) SK (Completed) BE (Completed) EE (Completed) FI (Completed) HU (Completed) DK (Completed) DE (Completed) CZ (Completed) ES (Completed) SE (Completed) AT (Completed) PT (Completed) NL (Completed) LV (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003075-12 | Sponsor Protocol Number: 290478 | Start Date*: Information not available in EudraCT |
Sponsor Name:Department Of Paediatric Cardiology | ||
Full Title: Effect of carvedilol on left ventricular systolic and diastolic function and the neurohormonal axis in patients with Duchenne muscular dystrophy and left ventricular dysfunction. | ||
Medical condition: Duchenne muscular dystrophy is an X-linked inherited disorder which primarily affects skeletal muscle through a mutation in dystrophin which maps to the long arm of the X chromosome (Xp21). Patient... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: IE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002520-33 | Sponsor Protocol Number: SNT-II-1 | Start Date*: 2005-09-06 |
Sponsor Name:Santhera Pharmaceuticals LLC | ||
Full Title: A Phase IIa double blind, randomised, placebo controlled, single centre study at the university of Leuven to assess the efficacy and tolerability of idebenone in 10 - 16 year old males with cardiac... | ||
Medical condition: Duchenne Muscular Dystrophy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004683-38 | Sponsor Protocol Number: G113 | Start Date*: 2015-01-26 | ||||||||||||||||||||||||||
Sponsor Name:Fondazione per il Tuo cuore onlus-ANMCO | ||||||||||||||||||||||||||||
Full Title: Effects of the dipeptidyl peptidase-4 (DPP-4) inhibitor linagliptin on left ventricular myocardial DYsfunction in patients with type 2 DiAbetes mellitus and concentric left ventricular geometry. | ||||||||||||||||||||||||||||
Medical condition: Type 2 Diabetes mellitus | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001005-27 | Sponsor Protocol Number: 1818 | Start Date*: 2011-05-02 | |||||||||||
Sponsor Name:Department of Anaesthesiology, University Hospital of Skejby | |||||||||||||
Full Title: The effect of dobtutamin on postoperative systolic deformation and diastolic function in patients with concentric hypertrophy of the left ventricle | |||||||||||||
Medical condition: Aortic stenosis Diastolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003273-42 | Sponsor Protocol Number: 14AOI11 | Start Date*: 2014-12-23 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Comparing a diuretic vascular filling in the initial management of acute pulmonary embolism with right ventricular dysfunction normotensive | |||||||||||||
Medical condition: acute pulmonary embolism with right ventricular dysfunction normotensive | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002269-21 | Sponsor Protocol Number: 01.00240 | Start Date*: 2013-12-06 |
Sponsor Name:Department of Physiology and Cardiothoracic Surgery, Faculty of Medicine, University of Porto | ||
Full Title: Metformin in diastolic dysfunction of metabolic syndrome | ||
Medical condition: Diastolic dysfunction in non-diabetic patients with metabolic syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002627-15 | Sponsor Protocol Number: BAY94-8862/14564 | Start Date*: 2013-05-27 | |||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||
Full Title: A randomized, double-blind, double-dummy, multi-center study to assess safety and efficacy of BAY 94-8862 in subjects with emergency presentation at the hospital because of worsening chronic heart ... | |||||||||||||||||||||||
Medical condition: Subjects with worsening chronic heart failure (WCHF) and left ventricular systolic dysfunction and either type 2 diabetes mellitus (DM type 2) with or without chronic kidney disease (CKD) or modera... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Completed) AT (Completed) SE (Completed) LT (Completed) DE (Completed) HU (Completed) CZ (Completed) NO (Completed) NL (Completed) PT (Completed) DK (Completed) IT (Completed) ES (Completed) BG (Completed) GR (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001196-46 | Sponsor Protocol Number: OPHT-240215 | Start Date*: 2015-05-15 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Effect of simvastatin withdrawal on ocular endothelial function | |||||||||||||
Medical condition: endothelial dysfunction in cardiovascular diseases | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002057-34 | Sponsor Protocol Number: PRePED-01 | Start Date*: 2020-02-07 | |||||||||||
Sponsor Name:Fundación de Investigación Biomédica Hospital Puerta de Hierro | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND CONTROLLED TRIAL TO EVALUATE THE EFFICACY OF INTRACAVERNOSAL INFUSION OF PLATELET RICH PLASMA (PRP) AGAINST PLATELET POOR PLASMA (PPP) IN THE TREATMENT OF VASCULOGENIC ER... | |||||||||||||
Medical condition: Vascular Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001704-37 | Sponsor Protocol Number: CSPP100A2340 | Start Date*: 2006-11-03 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 36 week, multicenter, randomized, double-blind, placebo- controlled, parallel-group, pilot study to evaluate the efficacy and safety of aliskiren on the prevention of left ventricular remodeling ... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) DK (Completed) DE (Completed) SE (Completed) BE (Completed) CZ (Completed) HU (Completed) GB (Completed) SK (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000191-15 | Sponsor Protocol Number: CORO-RYC-001 | Start Date*: 2018-06-13 | |||||||||||
Sponsor Name:IRICYS- Fundación para la Investigación Biomédica del Hospital Universitario Ramón y Cajal | |||||||||||||
Full Title: Effectiveness and Safety on Cardiac Frecuency Control With Ivabradine on the Cardiogenic Shock. (ES-FISH) | |||||||||||||
Medical condition: Cardiogenic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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