- 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 2 of 26.
EudraCT Number: 2015-005607-92 | Sponsor Protocol Number: QUIDHF_v3.0_20161130 | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:QUANTUM GENOMICS | |||||||||||||
Full Title: A Phase II randomized, placebo controlled, double-blind, multi-centre study to assess safety and efficacy of incremental doses of QGC001 in patients upon discharge or following hospitalization for ... | |||||||||||||
Medical condition: Patient with worsening chronic heart failure with left ventricular systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) NO (Completed) GB (Prematurely Ended) PL (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001433-83 | Sponsor Protocol Number: IMPROVE-AHF | Start Date*: 2015-01-15 | |||||||||||
Sponsor Name:Fundación INCLIVA | |||||||||||||
Full Title: Loop Diuretics Dosage in Patients with Acute Heart Failure and Renal Failure: Conventional versus Carbohydrate Antigen 125 guided Strategy | |||||||||||||
Medical condition: Acute Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001262-35 | Sponsor Protocol Number: D1690C00078 | Start Date*: 2023-02-09 | |||||||||||
Sponsor Name:The Brigham and Women's Hospital, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel Group, Placebo-Controlled Trial to Evaluate the Effect of In-Hospital Initiation of Dapagliflozin on Clinical Outcomes in Patients Who Have Been St... | |||||||||||||
Medical condition: The study is evaluating the effect of In-hospital initiation of dapagliflozin in patients who have been stabilized during hospitalization for Acute Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001613-33 | Sponsor Protocol Number: BRIDGE | Start Date*: 2014-05-13 | ||||||||||||||||
Sponsor Name:Thoraxclinic at the University of Heidelberg | ||||||||||||||||||
Full Title: Iloprost for Bridging to Heart Transplantation in Patients with Pulmonary Hypertension and Left Heart Failure | ||||||||||||||||||
Medical condition: Pulmonary Hypertension and Left Heart Failure | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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 |
EudraCT Number: 2006-001637-18 | Sponsor Protocol Number: CKI- 302 | Start Date*: 2006-11-13 | |||||||||||
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: SE (Completed) FI (Completed) CZ (Completed) BE (Completed) DK (Prematurely Ended) GB (Completed) HU (Completed) DE (Completed) NL (Completed) IT (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: 2007-004271-19 | Sponsor Protocol Number: RLX.CHF.003 | Start Date*: 2008-02-26 | |||||||||||
Sponsor Name:Corthera, Inc. | |||||||||||||
Full Title: A Phase II/III, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Relaxin in Subjects With Acute Heart Failure. | |||||||||||||
Medical condition: Patients hospitalized with Acute Heart Failure (AHF), normal to elevated blood pressure, and mild to moderate renal impairment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) IT (Completed) DE (Completed) FR (Completed) GB (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000763-18 | Sponsor Protocol Number: ACITRIM | Start Date*: 2007-02-20 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: ACUTE CHANGES OF ENERGETIC SUBSTRATES ON MIOCARDIAL FUNCTION AND METABOLISM, IN PATIENTS WITH CRONIC HEART FAILURE ACITRIM | |||||||||||||
Medical condition: HEART FAILURE | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002513-35 | Sponsor Protocol Number: CRLX030A3301 | Start Date*: 2013-11-28 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, prospective, randomized, open label study to assess the effect of serelaxin versus standard of care in acute heart failure (AHF) patients. | ||
Medical condition: Acute heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) BE (Completed) PT (Prematurely Ended) BG (Completed) LT (Completed) PL (Prematurely Ended) LV (Prematurely Ended) EE (Completed) FI (Prematurely Ended) SI (Prematurely Ended) GR (Prematurely Ended) ES (Prematurely Ended) HR (Prematurely Ended) DK (Prematurely Ended) IS (Prematurely Ended) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003048-37 | Sponsor Protocol Number: HSJC-CAR-01-2015 | Start Date*: 2015-11-13 |
Sponsor Name:Juan Luis Bonilla Palomas | ||
Full Title: Effect of ?-3 polyunsaturated fatty acids on serum albumin concentration in patients with acute heart failure, hypoalbuminemia, and high inflammatory activity | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
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: 2010-021003-24 | Sponsor Protocol Number: 20100754 | Start Date*: 2011-07-28 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of IV Infusion Treatment With Omecamtiv Mecarbil in Subjects With Left Ventricular Systolic Dys... | |||||||||||||
Medical condition: Acute heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) GB (Completed) LT (Completed) FI (Prematurely Ended) SK (Completed) CZ (Completed) HU (Completed) PL (Completed) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002893-76 | Sponsor Protocol Number: PRAGUE-10 | Start Date*: 2008-02-13 |
Sponsor Name:Charles University in Prague, Third Faculty of Medicine | ||
Full Title: MEtabolic Therapy with Trimetazidine in Acute heart failure: an open pilot randomized trial (The METTA – PRAGUE 10 Trial) | ||
Medical condition: Acute Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022952-22 | Sponsor Protocol Number: GIU-LU-RO | Start Date*: 2010-10-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: N-Acetytilcysteine Versus placebo for the prevention of Acute Reduction in Renal function after primary Angioplasty (NoVARA) | |||||||||||||
Medical condition: patient with ST elevation myocardial acute infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000588-26 | Sponsor Protocol Number: ICCE12.001 | Start Date*: 2012-10-16 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Pharmacokinetics of Levosimendan in children with acute heart failure | ||
Medical condition: Acute heart failure in children | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) FI (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019710-24 | Sponsor Protocol Number: QoLESS-AZA-AMLE | Start Date*: 2010-09-01 | |||||||||||
Sponsor Name:ASSOCIAZIONE QOL-ONE | |||||||||||||
Full Title: A Randomized Study to Evaluate the Efficacy of 5-Aza for Post-Remission Therapy of Acute Myeloid Leukemia in Elderly Patients (QoLESS AZA-AMLE) | |||||||||||||
Medical condition: ACUTE MYELOID LEUKEMIA PATIENTS | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005054-30 | Sponsor Protocol Number: CamiciSerelaxin2013_CRLX030AIT01T | Start Date*: 2014-06-10 | |||||||||||
Sponsor Name:Ospedale San Raffaele s.r.l. | |||||||||||||
Full Title: A mechanistic study to evaluate the effect of Serelaxin on left ventricular function and its correlation with outcome in acute heart failure | |||||||||||||
Medical condition: Acute 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: 2022-003206-69 | Sponsor Protocol Number: ASST-FARM-CAR_STEROHF-2022 | Start Date*: 2023-01-30 | |||||||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||||||||||||
Full Title: A multicenter, randomized, open-label, controlled study to evaluate the efficacy and safety of corticoSTEROids added to standard therapy in patients with Acute Heart Failure (STERO-AHF) | |||||||||||||||||||||||
Medical condition: patients with Acute 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: 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) |
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