- 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 3 of 26.
EudraCT Number: 2019-003902-29 | Sponsor Protocol Number: EASI-Child | Start Date*: 2020-04-30 | |||||||||||
Sponsor Name:IRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA | |||||||||||||
Full Title: Early Administration of Ivabradine in Children with Heart Failure. | |||||||||||||
Medical condition: Acute hearth failure in dilated cardiomyopathy. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003314-37 | Sponsor Protocol Number: CCM1862 | Start Date*: 2023-04-19 | |||||||||||
Sponsor Name:CENTRO CARDIOLOGICO SPA FONDAZIONE MONZINO | |||||||||||||
Full Title: Effects of combined diuretic therapy on exercise capacity, alveolus-capillary diffusion, and maintenance of euvolemia in chronic congestive heart failure, diuretic therapy compared between loop diu... | |||||||||||||
Medical condition: congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002946-19 | Sponsor Protocol Number: 1245-0204 | Start Date*: 2020-01-15 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: A multicentre, randomised, double-blind, 90-day superiority trial to evaluate the effect on clinical benefit, safety and tolerability of once daily oral EMPagliflozin 10 mg compared to placebo, ini... | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) NL (Completed) BE (Completed) DE (Completed) DK (Completed) ES (Completed) HU (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001407-37 | Sponsor Protocol Number: CKI- 301 | Start Date*: 2007-06-20 | |||||||||||
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: DE (Completed) GB (Completed) CZ (Completed) HU (Completed) IT (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004488-20 | Sponsor Protocol Number: FURO-HGUA-08/01 | Start Date*: 2009-05-08 | |||||||||||
Sponsor Name:HOSPITAL GENERAL UNIVERSITARIO DE ALICANTE | |||||||||||||
Full Title: Ensayo clínico en fase IV, multicéntrico, controlado, aleatorizado, para evaluar la eficacia y seguridad de 3 pautas de administración de furosemida en pacientes con descompensación aguda moderada-... | |||||||||||||
Medical condition: Descompensación aguda moderada-severa en pacientes con insuficiencia cardíaca congestiva (Acute moderate to severe descompensation in patients with congestive heart failure) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006843-29 | Sponsor Protocol Number: CKI-303 | Start Date*: 2007-06-13 | |||||||||||
Sponsor Name:NovaCardia Inc | |||||||||||||
Full Title: A multicentre, randomized, double-blind, placebo controlled study of the effects of KW-3902 Injectable Emulsion on heart failure signs and symptoms, diuresis, renal function, and clinical outcomes ... | |||||||||||||
Medical condition: Patients being admitted to hospital with heart failure and volume overload requiring IV therapy after experiencing worsening of renal function. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) IT (Completed) PL (Completed) GR (Completed) BE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018353-36 | Sponsor Protocol Number: FARM8PRTEC | Start Date*: 2010-05-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA` GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: BeTACTIC Study. Best Therapy After Cardiac Transplantation, the Italian Challenge. A multicenter, prospective, randomized, open-label study to compare the efficacy and safety of Everolimus and Myc... | |||||||||||||
Medical condition: Paitents will be enrolled at least one year after heart transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003059-36 | Sponsor Protocol Number: Bay 58-2667/12480 | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: Placebo controlled, randomized, double-blind, multi-center, multinational Phase IIb study to investigate the efficacy and tolerability of BAY 58-2667 given intravenously in patients with acute deco... | |||||||||||||
Medical condition: Patients with acute decompensated chronic congested heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) IT (Prematurely Ended) SE (Prematurely Ended) EE (Prematurely Ended) CZ (Prematurely Ended) ES (Prematurely Ended) SI (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000771-24 | Sponsor Protocol Number: CXL-1427-02 | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Cardioxyl Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase IIa Study of the Safety, Tolerability and Hemodynamic Effects of a Continuous 6-Hour Intravenous Infusion of CXL-1427 in Hospitalized Patients with Systolic Heart Failure | |||||||||||||
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: View results |
EudraCT Number: 2006-002403-13 | Sponsor Protocol Number: Ularitide-1502 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:PDL BioPharma Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blinded, Placebo-controlled Study of Ularitide in the Treatment of Subjects with Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) LT (Prematurely Ended) AT (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003497-48 | Sponsor Protocol Number: EMPATHY | Start Date*: 2021-11-29 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: Empagliflozin and dapagliflozin in patients hospitalized for acute decompensated heart failure (EMPATHY) – a phase III trial | |||||||||||||
Medical condition: acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003688-37 | Sponsor Protocol Number: KKS-243 | Start Date*: 2018-07-06 | ||||||||||||||||
Sponsor Name:Philipps-Universität Marburg | ||||||||||||||||||
Full Title: Phosphodiesterase-5 inhibition in patients with heart failure with preserved ejection fraction and combined post- and pre-capillary pulmonary hypertension (PASSION), A randomized, placebo-controll... | ||||||||||||||||||
Medical condition: Combined post- and pre-capillary pulmonary hypertension and heart failure with preserved ejection fraction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: 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: 2015-001611-12 | Sponsor Protocol Number: 56022473AML2002 | Start Date*: 2015-07-03 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized Phase 2/3 Study of DACOGEN® (Decitabine) Plus JNJ-56022473 (Anti-CD123) Versus DACOGEN (Decitabine) Alone in Patients with AML who are not Candidates for Intensive Chemotherapy | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) SE (Completed) PL (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001853-89 | Sponsor Protocol Number: CLI-043 | Start Date*: 2006-07-07 |
Sponsor Name:Vion Pharmaceuticals, Inc | ||
Full Title: A phase II study of Cloretazine for elderly patients with de novo poor risk acute myelogenous leukemia. | ||
Medical condition: Acute Myelogenous Leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: (No results available) |
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: 2016-001467-36 | Sponsor Protocol Number: FER-CARS-06 | Start Date*: 2017-02-02 | |||||||||||||||||||||
Sponsor Name:Vifor (International) Inc. | |||||||||||||||||||||||
Full Title: A Randomised, Double-blind Placebo Controlled Trial Comparing the Effect of Intravenous Ferric Carboxymaltose on Hospitalisations and Mortality in Iron Deficient Patients Admitted for Acute Heart F... | |||||||||||||||||||||||
Medical condition: Acute heart failure with iron deficiency | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) NL (Completed) PL (Completed) HR (Completed) SE (Completed) ES (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-004186-21 | Sponsor Protocol Number: VICTORID_01 | Start Date*: 2023-09-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Dipartimento di Medicina-DIMED, università di Padova | |||||||||||||||||||||||||||||||||
Full Title: Beneficial effects of vitamin D combined with oral iron supplementation in patients with chronic heart failure and iron deficiency (VICTORID-HF TRIAL) | |||||||||||||||||||||||||||||||||
Medical condition: Chronic heart failure; iron deficiency | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002042-32 | Sponsor Protocol Number: CPX-351-TA-SMP | Start Date*: 2021-09-16 | |||||||||||
Sponsor Name:FILO | |||||||||||||
Full Title: A phase II study of CPX-351 monotherapy in Acute Myeloid Leukemia secondary to Myeloproliferative neoplams | |||||||||||||
Medical condition: newly secondary AML according to WHO 2016 classification following an antecedent of Myeloproliferative Neoplasm including Essential Thrombocythemia (ET), Polycythemia Vera (PV), primary or secondar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003786-20 | Sponsor Protocol Number: S320.2.011 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Solvay Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Randomized, Multi-Center, Dose-Finding Study of SLV320, a Selective A1 Adenosine Receptor Antagonist, to Evaluate the Effect on Renal Function and Safety in Subj... | |||||||||||||
Medical condition: Acute Decompensated Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) DK (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
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