- Trials with a EudraCT protocol (2,578)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,578 result(s) found for: Heart Diseases.
Displaying page 7 of 129.
EudraCT Number: 2014-004592-23 | Sponsor Protocol Number: DLIFE | Start Date*: 2015-03-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: Phase IV randomized, double blind, placebo-controlled study: role of hypovitaminosis D in heart failure and possible advantages of cholecalciferol (Vit D) administration | |||||||||||||
Medical condition: HEART FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001700-37 | Sponsor Protocol Number: CELL-004 | Start Date*: 2012-10-03 | |||||||||||
Sponsor Name:Celladon Corporation | |||||||||||||
Full Title: A Phase 2b, Double-Blind, Placebo-Controlled, Multinational, Multicenter, Randomized Study Evaluating the Safety and Efficacy of Intracoronary Administration of MYDICAR® (AAV1/SERCA2a) in Subjects ... | |||||||||||||
Medical condition: Moderate to advanced heart failure (NYHA class II, III or IV) due to systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) GB (Completed) BE (Completed) PL (Completed) NL (Completed) DK (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001623-39 | Sponsor Protocol Number: Levo1010 | Start Date*: 2018-07-26 |
Sponsor Name:Verein zur Förderung der Forschung auf dem Gebiet der Arteriosklerose, Thrombose und vaskulären Biologie (ATVB) | ||
Full Title: Assessment of body composition changes after Levosimendan treatment in patients with advanced heart failure | ||
Medical condition: Advanced heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000376-28 | Sponsor Protocol Number: 1245.148 | Start Date*: 2018-01-30 | |||||||||||
Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, mechanistic cardiac magnetic resonance study to investigate the effects of empagliflozin treatment on cardiac physiology and metabolism in patients w... | |||||||||||||
Medical condition: Chronic heart failure with reduced (HFrEF) and preserved ejection fraction (HFpEF) diagnosed at least 3 months prior to informed consent. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020376-37 | Sponsor Protocol Number: CP120027.2001 | Start Date*: 2011-02-11 | |||||||||||||||||||||||||||||||
Sponsor Name:Trevena, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Adaptive, Ascending Dose-Titration Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Invasive Hemodynamics of TRV120027 in Patient... | |||||||||||||||||||||||||||||||||
Medical condition: Heart failure | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004154-25 | Sponsor Protocol Number: CLCZ696B2319E1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter study to evaluate long-term safety and tolerability of open label sacubitril/valsartan in pediatric patients with heart failure due to systemic left ventricle systolic dysfunction wh... | |||||||||||||
Medical condition: Pediatric heart failure : Patients (≥ 13 months) with HF due to systemic left ventricular systolic dysfunction. [Note: All patients per protocol for the core study CLCZ696B2319 (PANORAMA-HF) ... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) FR (Completed) BG (Completed) PT (Completed) CZ (Completed) ES (Ongoing) HU (Completed) HR (Completed) DE (Completed) AT (Completed) IT (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016498-13 | Sponsor Protocol Number: TIC-0911 | Start Date*: 2010-12-22 | |||||||||||
Sponsor Name:Fundación para la Formación en Investigación Sanitarias de la Región de Murcia | |||||||||||||
Full Title: Estudio aleatorizado y doble-ciego para valorar el beneficio del tratamiento con testosterona en pacientes deficientes con IC avanzada (TIC) | |||||||||||||
Medical condition: Deficiencia de testorena en varones con insuficiencia cardiaca. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003119-39 | Sponsor Protocol Number: 38RC15.175 | Start Date*: 2015-10-29 | ||||||||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Grenoble | ||||||||||||||||||
Full Title: effects of a short therpay of zolpidem with support servo-ventilation versus placebo in patients with central sleep apnea with chronic heart failure | ||||||||||||||||||
Medical condition: chronic heart failure and central sleep apnea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001784-77 | Sponsor Protocol Number: ML6721 | Start Date*: 2012-05-07 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Fontan patients: Comprehensive evaluation of the pulmonary circulation to identify pulmonary vascular disease and its influence on ventricular hemodynamics. | |||||||||||||
Medical condition: Fontan patients | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022529-14 | Sponsor Protocol Number: WC25501 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche | |||||||||||||
Full Title: A phase III, double-blind, randomized, placebo-controlled, multi-center study evaluating the efficacy and safety of dalcetrapib on lipids, lipoproteins, apolipoproteins and markers of CV risk in pa... | |||||||||||||
Medical condition: Coronary Heart Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2020-004877-38 | Sponsor Protocol Number: PREVENT-MINS | Start Date*: 2021-06-18 | |||||||||||
Sponsor Name:Uniwersytet Jagielloński - Collegium Medicum | |||||||||||||
Full Title: Ivabradine for PREVENTion of Myocardial Injury after Noncardiac Surgery (MINS) - PREVENT-MINS Trial | |||||||||||||
Medical condition: Myocardial Injury after Noncardiac Surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002522-23 | Sponsor Protocol Number: BAY1067197/16782 | Start Date*: 2013-12-20 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A double blinded, placebo controlled, study to investigate the safety, tolerability, pharmacokinetics and acute cardiovascular responses of a 7 day oral treatment with the partial adenosine A1 rece... | |||||||||||||
Medical condition: Chronic systolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000269-27 | Sponsor Protocol Number: DSCK101 | Start Date*: 2014-11-06 |
Sponsor Name:German Foundation for Chronically Ill | ||
Full Title: Efficacy and tolerance of Beta Blocker and Procoralan uptitration in chronic heart failure patients under telemedical control: „70 bpm on day 28“ | ||
Medical condition: Patients with chronic heart failure and resting heart rate of ≥ 75 bmp | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000220-33 | Sponsor Protocol Number: CLCZ696BDE03 | Start Date*: 2019-02-04 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, double-blind, active-controlled study to assess the effect of sacubitril/valsartan compared with enalapril to improve erectile function in patients with heart failure with reduced eje... | |||||||||||||
Medical condition: Patients with heart failure with reduced ejection fraction (HFrEF) and erectile dysfunction (ED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022821-14 | Sponsor Protocol Number: 2010-022821-14 | Start Date*: 2010-11-11 | ||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||||||||||||||||||
Full Title: Cardiovascular Outcomes of Replacement with Testosterone. Role of testosterone replacement therapy in patients with heart failure. | ||||||||||||||||||
Medical condition: MALE HYPOGONADISM | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002912-25 | Sponsor Protocol Number: 1VIT15043 | Start Date*: 2019-11-18 | ||||||||||||||||
Sponsor Name:American Regent, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Injectafer® (Ferric Carboxymaltose) as Treatment for Heart Failure with Iron Deficiency | ||||||||||||||||||
Medical condition: Heart Failure with Iron Deficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) HU (Completed) CZ (Completed) LT (Completed) LV (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000413-48 | Sponsor Protocol Number: 8.1(IRE),2017.03.24 | Start Date*: 2015-07-01 |
Sponsor Name:ACS Biomarker | ||
Full Title: Bioprofiling response to mineralocorticoid receptor antagonists for the prevention of heart failure. A proof of concept clinical trial within the EU FP 7 “HOMAGE” programme « Heart OMics in AGing | ||
Medical condition: Elderly patients with Clinical and Biological risk factors for developing heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) DE (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003111-28 | Sponsor Protocol Number: REPO-HFpEF-II | Start Date*: 2023-02-15 | |||||||||||
Sponsor Name:Hospital Clínico Universitario de Valencia | |||||||||||||
Full Title: Mechanism-based drug REpurPOsing in a subtype of Heart Failure with Preserved Ejection Fraction (REPO-HFPEF) | |||||||||||||
Medical condition: Subtype of Heart Failure with Preserved Ejection Fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015712-17 | Sponsor Protocol Number: G080186 | Start Date*: 2010-03-25 | |||||||||||
Sponsor Name:HCRI | |||||||||||||
Full Title: A prospective, multi-center, randomized, double-blind trial to assess the effectiveness and safety of 12 versus 30 months of dual antiplatelet therapy (DAPT) in subjects undergoing percutaneous cor... | |||||||||||||
Medical condition: Dual antiplatelet therapy (DAPT) in subjects undergoing percutaneous coronary intervention (PCI) with either drug eluting stent (DES) or bara metal stent (BMS) placement for the treatment of corona... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) DE (Completed) CZ (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000486-37 | Sponsor Protocol Number: CHF201701 | Start Date*: 2019-03-27 |
Sponsor Name:Heart Initiative | ||
Full Title: STRONG-HF: Safety, Tolerability and efficacy of Rapid Optimization, helped by NT-proBNP testing, of Heart Failure therapies | ||
Medical condition: Acute Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) HR (Completed) | ||
Trial results: View results |
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