- Trials with a EudraCT protocol (1,477)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,477 result(s) found for: Heart Failure.
Displaying page 1 of 74.
EudraCT Number: 2008-001850-42 | Sponsor Protocol Number: MSC3 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:The Heart Centre, Rigshospitalet | |||||||||||||
Full Title: Autolog mesenkymal stromal cellebehandling af patienter med hjertesvigt. | |||||||||||||
Medical condition: Congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002688-31 | Sponsor Protocol Number: ICOR-2022-04-LEVOMEMS | Start Date*: 2023-01-25 | ||||||||||||||||||||||||||
Sponsor Name:Germans Trias i Pujol Health Research Institute | ||||||||||||||||||||||||||||
Full Title: LEVO-MEMS: COMPARISION OF THE HAEMODINAMIC PROFILE OF DOBUTAMIN AND LEVOSIMENDAN IN THE CURRENT THERAPEUTICAL CONTEXT | ||||||||||||||||||||||||||||
Medical condition: Heart failure patients with depressed left ventricular ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001134-33 | Sponsor Protocol Number: iCHF | Start Date*: 2012-11-21 | |||||||||||
Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled Trial of Ferric Carboxymaltose Versus Placebo in Patients with Congestive Heart Failure | |||||||||||||
Medical condition: Congestive heart failure (CHF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004727-10 | Sponsor Protocol Number: 12345 | Start Date*: 2006-11-14 | |||||||||||
Sponsor Name:Kuopion Yliopistollinen Sairaala | |||||||||||||
Full Title: Teofylliinin vaikutus sydämen oikean puolen toimintaan - randomisoitu, kaksoissokkoutettu, plasebokontrolloitu hemodynaaminen invasiivinen (PAC) ja echokardiografinen tutkimus | |||||||||||||
Medical condition: Sydänleikkauksen jälkeinen subkliininen sydämen oikean puolen vajaatoiminta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021263-33 | Sponsor Protocol Number: 3001101 | Start Date*: 2011-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Sykehuset i Vestfold HF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: PERIOPERATIVE LEVOSIMENDAN INFUSION IN PATIENTS WITH HEART FAILURE UNDERGOING NON-CARDIAC SURGERY: A PROSPECTIVE, RANDOMISED, PLACEBO-CONTROLLED, DOUBLE-BLIND, MULTICENTER STUDY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with serious cardiac failure scheduled for non-cardiac surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004487-22 | Sponsor Protocol Number: BMI 001 / SMR-1389 | Start Date*: 2005-11-25 | |||||||||||
Sponsor Name:Bio-Medisinsk Innovasjon AS | |||||||||||||
Full Title: A Proof of Biological Efficacy Study Assessing the Potential of Piboserod a Specific 5-HT4 Antagonist for the Treatment of Symptomatic Congestive Heart Failure in stable outpatients NYHA class II-I... | |||||||||||||
Medical condition: Congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006237-27 | Sponsor Protocol Number: CT/P004/HF/08/02_01 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Torrent Pharmaceuticals Ltd. | |||||||||||||
Full Title: Safety and efficacy of TRC4186 in the treatment of stable heart failure associated with HbA1c >= 6 % or type 2 diabetes receiving oral hypoglycaemic therapy (with or without additional insulin) as ... | |||||||||||||
Medical condition: heart failure associated with impaired glucose tolerance or type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001971-30 | Sponsor Protocol Number: CLCZ696B2317 | Start Date*: 2014-11-22 | |||||||||||
Sponsor Name:Novartis Pharma services AG | |||||||||||||
Full Title: A multicenter study to evaluate safety and tolerability in patients with chronic heart failure and reduced ejection fraction from PARADIGM-HF receiving open label LCZ696 | |||||||||||||
Medical condition: Heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) FI (Completed) NL (Completed) CZ (Completed) SE (Completed) SK (Completed) HU (Completed) PT (Completed) DK (Completed) EE (Completed) ES (Completed) IT (Completed) DE (Completed) BE (Completed) BG (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001560-19 | Sponsor Protocol Number: CSCC-ASC2 | Start Date*: 2015-06-29 | |||||||||||
Sponsor Name:Department of Cardiology, Rigshospitalet | |||||||||||||
Full Title: Allogeneic adipose tissue-derived stromal/stem cell therapy in patients with ischemic heart disease and heart failure | |||||||||||||
Medical condition: Ischemic heart disease and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001109-28 | Sponsor Protocol Number: pgrf/141/09 | Start Date*: 2008-05-23 | |||||||||||||||||||||
Sponsor Name:University of Aberdeen | |||||||||||||||||||||||
Full Title: Perhexiline therapy in patients with heart failure with preserved left ventricular ejection fraction(HFpEF syndrome) | |||||||||||||||||||||||
Medical condition: Heart failure with preserved left ventricular ejection fraction | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016364-36 | Sponsor Protocol Number: P09 | Start Date*: 2010-07-06 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Injection of Autologous Bone Marrow Cells into Damaged Myocardium of No-option Patients with Ischemic Heart Failure: a randomized placebo controlled trail. | |||||||||||||
Medical condition: Ischemic heart failure is associated with significant morbidity and mortality. The number of patients with severe heart failure that remains symptomatic despite optimal pharmacological and non-phar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004600-53 | Sponsor Protocol Number: RBK03-16-00389 | Start Date*: 2018-06-08 | ||||||||||||||||||||||||||
Sponsor Name:WÖRWAG Pharma GmbH & Co. KG | ||||||||||||||||||||||||||||
Full Title: MACH 2 - Magnesium orotate in severe congestive heart failure - Part 2 | ||||||||||||||||||||||||||||
Medical condition: Heart failure with reduced ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001287-34 | Sponsor Protocol Number: BAY1067197/16718 | Start Date*: 2013-11-04 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A single blind, placebo controlled pilot study to explore the safety and tolerability of a single oral dose of 30 mg BAY 1067197 in patients with chronic heart failure on the background of preexist... | |||||||||||||
Medical condition: Heart failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004805-29 | Sponsor Protocol Number: 201200480529 | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:The Heart Center, Rigshospitalet | |||||||||||||
Full Title: Beta 3 agonist treatment in heart failure (BEAT-HF) | |||||||||||||
Medical condition: Systolic heart failure | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000885-39 | Sponsor Protocol Number: 02289 | Start Date*: 2021-01-12 | |||||||||||
Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
Full Title: Safety and Efficacy of Induced Pluripotent Stem Cell-derived Engineered Human Myocardium as Biological Ventricular Assist Tissue in Terminal Heart Failure | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006337-19 | Sponsor Protocol Number: R5381-HF-2159 | Start Date*: 2022-06-08 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Doses of REGN5381, an NPR1 Agonis... | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004225-10 | Sponsor Protocol Number: 3001081 | Start Date*: 2005-03-07 | |||||||||||
Sponsor Name:Orion Pharma | |||||||||||||
Full Title: Effects of peroral levosimendan in the prevention of further hospitalisations in patients with chronic heart failure. A randomised, double-blind, placebo-controlled, multi-centre, parallel-group study | |||||||||||||
Medical condition: Cardiac Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LT (Completed) LV (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000046-19 | Sponsor Protocol Number: RIVAROXHFA3001/BAY59-7939/16302 | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Event-driven, Multicenter Study Comparing the Efficacy and Safety of Oral Rivaroxaban with Placebo for Reducing the Risk of Death, Myocardial Infarction or Stroke in Sub... | |||||||||||||
Medical condition: Prevention of death, heart attack and stroke in patients with chronic heart failure and significant coronary artery disease following a hospitalization for exacerbation of heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) NL (Completed) BG (Completed) PL (Completed) HU (Completed) SE (Completed) IT (Completed) GB (Completed) EE (Completed) LT (Completed) PT (Completed) DK (Completed) LV (Completed) SK (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002468-26 | Sponsor Protocol Number: DKprotokol(LIVE)v5 | Start Date*: 2011-08-12 | |||||||||||
Sponsor Name:Allan Flyvbjerg | |||||||||||||
Full Title: Liraglutide in chronic heart failure. A randomised, double-blind, placebo-controlled study of the effect of LIraglutide on left VEntricular function in chronic heart failure patients with and witho... | |||||||||||||
Medical condition: Primary objective: To investigate the effect of Liraglutide 1.8 mg once daily compared to placebo on left ventricular eject fraction in Chromic heart failure patients with and without Type 2 diabe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013103-63 | Sponsor Protocol Number: 1884 | Start Date*: 2011-12-14 | |||||||||||
Sponsor Name:Asklepios Kliniken Hamburg GmbH | |||||||||||||
Full Title: Pilot study investigating the effect of intra-coronary and intra-myocardial application of enriched CD133pos autologous bone marrow derived stem cells for improving left ventricular function in chr... | |||||||||||||
Medical condition: Patients with chronic ischemic cardiomyopathy with an LVEF ≤45% and symptomatic heart failure NYHA ≥ II under optimal therapy and drug treatment according to the current ESC heart failure guidelines. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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