- Trials with a EudraCT protocol (511)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
511 result(s) found for: Acute heart failure.
Displaying page 5 of 26.
EudraCT Number: 2014-003589-25 | Sponsor Protocol Number: Levo-AKI | Start Date*: 2014-11-11 |
Sponsor Name:Sahlgrenska Universitetssjukhuset/Sahlgrenska | ||
Full Title: The effect of levosimendan, on renal blood flow, function and oxygen uptake during acute renal failure after cardiac surgery | ||
Medical condition: Acute kidney injury postoperatively in connection with heart surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005713-40 | Sponsor Protocol Number: 69HCL20_1135 | Start Date*: 2021-08-02 |
Sponsor Name:Hospices Civils de Lyon | ||
Full Title: Acute Reno-Cardiac Action of Dapagliflozin In Advanced Heart Failure patients on heart transplant waiting list: a multicenter, double-blind, randomized clinical trial. | ||
Medical condition: for advanced Heart Failure patients on heart transplant waiting list | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2021-001466-37 | Sponsor Protocol Number: A-STAMI | Start Date*: 2021-07-08 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen, Sahlgrenska University Hospital | ||||||||||||||||||
Full Title: Adenosine’s effect on STunning resolution in Acute Myocardial Infarction | ||||||||||||||||||
Medical condition: Acute Myocardial Infarction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000130-33 | Sponsor Protocol Number: ORION-HF | Start Date*: 2022-12-23 | ||||||||||||||||||||||||||
Sponsor Name:Hannover Medical School | ||||||||||||||||||||||||||||
Full Title: A pilot study to explore safety, tolerability and efficacy of ORal IrON supplementation with ferric maltol in treating iron deficiency and anaemia in patients with Heart Failure (ORION-HF) | ||||||||||||||||||||||||||||
Medical condition: Patients with heart failure, iron deficiency and anaemia with either reduced or preserved left ventricular ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022763-35 | Sponsor Protocol Number: VITAMINDHeartFailure1.0 | Start Date*: 2011-03-31 |
Sponsor Name:Medical University of Graz | ||
Full Title: Vitamin D supplementation in chronic heart failure: a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Chronic stable heart failure (NYHA II-IV, ejection fraction ≤ 40%) Vitamin D deficiency (defined as 25 (OH) Vitamin D ≤ 30ng/ml) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003995-65 | Sponsor Protocol Number: TAKICARD-1 | Start Date*: 2015-11-25 | |||||||||||
Sponsor Name:Västra Götalandsregionen, Sahlgrenska University Hospital /Queen Silvia children's hospital | |||||||||||||
Full Title: Pharmacokinetics of ANP, a diuretic hormone, in neonates undergoing surgery for congenital heart defects. A pilot study. | |||||||||||||
Medical condition: Acute renal failure after heart surgery | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005310-19 | Sponsor Protocol Number: PI-0697-2012 | Start Date*: 2013-06-05 |
Sponsor Name:FUNDACION PARA LA INVESTIGACIÓN BIOSANITARIA DE ANDALUCIA ORIENTAL_ FPA | ||
Full Title: Double-blind randomized clinical trial to evaluate the efficacy and safety of levosimendan as preischemic myocardial conditioner in pediatric cardiac surgery | ||
Medical condition: Children aged 1 month to 14 years in the health area of the province of Granada who will be undergoing heart surgery with a clinical high risk of developing acute heart failure after surgery, treat... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001464-19 | Sponsor Protocol Number: GE-122-020 | Start Date*: 2016-02-11 | ||||||||||||||||
Sponsor Name:GE Healthcare Ltd. and its affiliates | ||||||||||||||||||
Full Title: AdreView™ Myocardial Imaging for Risk Evaluation – A multicentre trial to guide ICD implantation in NYHA class II & III heart failure patients with 30%≤LVEF≤35% ADMIRE-ICD | ||||||||||||||||||
Medical condition: Heart failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005098-29 | Sponsor Protocol Number: 2017PZY5K7 | Start Date*: 2021-07-09 | |||||||||||
Sponsor Name:DIPARTIMENTO DI MEDICINA CLINICA E CHIRURGIA - UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: Novel therapeutic strategies to reduce coronary microvascular obstruction and to OPTImize non-culprit stenoses revascularization in ST-Elevation acute Myocardial Infarction Randomized, no-profit, ... | |||||||||||||
Medical condition: Patients with acute ST-elevation myocardial infarction (STEMI) and multivessel coronary artery disease (MVD) defined by at least one non-culprit stenosis (NCS) with angiographic severity between 3... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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) |
EudraCT Number: 2020-002708-38 | Sponsor Protocol Number: 131313 | Start Date*: 2020-10-26 |
Sponsor Name:Department of Medical Science Gothenburg University | ||
Full Title: Optimized pharmacological treatment for broken heart (takotsubo) syndrome | ||
Medical condition: The medical condition is acute heart failure (Takotsubo syndrome) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002893-35 | Sponsor Protocol Number: CP027.2002 | Start Date*: 2013-11-21 |
Sponsor Name:Trevena Inc. | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Explore the Efficacy of TRV027 in Patients Hospitalized for Acute Decompensated Heart Failure | ||
Medical condition: Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) SK (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004772-18 | Sponsor Protocol Number: ASTX727-07 | Start Date*: 2022-05-30 | |||||||||||
Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Single-Arm, Open-Label Pharmacokinetic, Safety, and Efficacy Study of ASTX727 in Combination with Venetoclax in Adult Patients with Acute Myeloid Leukemia | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000885-40 | Sponsor Protocol Number: 04-CL-1904 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:Windtree Therapeutics, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study on the Safety and Efficacy of Istaroxime for Pre-Cardiogenic Shock (SEISMiC) | |||||||||||||
Medical condition: Pre-Cardiogenic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002847-28 | Sponsor Protocol Number: CRLX030A2208 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Multicenter, open-label, dose escalation study to evaluate safety, tolerability and pharmacokinetics of RLX030 in addition to standard of care in pediatric patients from birth to <18 years of age, ... | |||||||||||||
Medical condition: acute heart failure | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003559-39 | Sponsor Protocol Number: 2011PP02 | Start Date*: 2013-10-01 | |||||||||||
Sponsor Name:The University of Dundee [...] | |||||||||||||
Full Title: Allopurinol and cardiovascular outcomes in patients with ischaemic heart disease (ALL-HEART) | |||||||||||||
Medical condition: Ischaemic Heart Disease (IHD), angina or myocardial infarction | |||||||||||||
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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: 2005-000837-39 | Sponsor Protocol Number: CCD01 | Start Date*: 2007-08-15 | |||||||||||
Sponsor Name:Cytonet GmbH & Co. KG | |||||||||||||
Full Title: Open, randomized, prospective, controlled, multicentre study to evaluate the efficacy and safety of multiple intraportal applications of liver cell suspension in patients with acute liver failure n... | |||||||||||||
Medical condition: Acute Liver Failure Subgroups of patients with indications falling under ICD classification codes:K70.4, K71, K72, K75, K76, K77 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004977-10 | Sponsor Protocol Number: 08meInnereA_GALACTIC | Start Date*: 2013-07-25 | |||||||||||||||||||||
Sponsor Name:University Hospital Basel, Cardiology | |||||||||||||||||||||||
Full Title: Goal-directed Afterload Reduction in Acute Congestive Cardiac Decompensation Study | |||||||||||||||||||||||
Medical condition: - acute decompensated heart failure | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prohibited by CA) BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003949-11 | Sponsor Protocol Number: GS-US-546-5857 | Start Date*: 2021-11-05 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Open-Label Study Evaluating the Safety and Efficacy of Magrolimab in Combination with Azacitidine versus Physician’s Choice of Venetoclax in Combination with Azacitidine or I... | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) DE (Completed) SE (Completed) FR (Completed) ES (Prematurely Ended) IT (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002431-80 | Sponsor Protocol Number: LEV1068 | Start Date*: 2006-09-15 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Renal Effects of Levosimendan in Patients Admitted with Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Patients with acute decompensated heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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