- 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 7 of 26.
EudraCT Number: 2004-001225-16 | Sponsor Protocol Number: 3001077 | Start Date*: 2004-10-28 |
Sponsor Name:Orion Pharma | ||
Full Title: Survival of patients with acute heart failure in need of intravenous inotropic support; a multicentre parallel- group, randomised, double- blind, double- dummy study of levosimendan versus dobutami... | ||
Medical condition: Acutely decompensated heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001840-37 | Sponsor Protocol Number: 2017-001840-37 | Start Date*: 2019-01-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: ERtugliflozin triAl in DIabetes with preserved or reduced ejeCtion FrAcTion mEchanistic evaluation in Heart Failure: "ERADICATE-HF" | ||
Medical condition: Diabetes Mellitus Type 2 and Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014378-16 | Sponsor Protocol Number: Bay 58-2667/14663 | Start Date*: 2010-01-14 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A Placebo Controlled, Randomized, Double-Blind, Fixed-dose, Multicenter, Phase IIb Study to Investigate the Efficacy and Tolerability of Low Dose BAY 58-2667 (25 μg/h, 10 μg/h) Given Intravenously ... | |||||||||||||
Medical condition: Acute Decompensated Chronic Congestive Heart Failure (ADHF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IE (Prematurely Ended) AT (Prematurely Ended) FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003573-32 | Sponsor Protocol Number: 2022/ABM/01/00027 | Start Date*: 2023-12-28 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the effect of allopurinol on the risk of cardiovascular events in patients at high and very high cardiovascular risk, including the ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: hyperuricemia, hypertension, ischemic stroke, intracerebral haemorrhage, TIA, heart failure, peripheral arterial disease, atrial fibrillation, diabetes mellitus | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2007-003866-16 | Sponsor Protocol Number: AP REN 01-01 | Start Date*: 2009-03-03 | ||||||||||||||||
Sponsor Name:AM-Pharma B.V. | ||||||||||||||||||
Full Title: A Phase-II, double-blind, randomized, placebo-controlled proof of concept study on the safety and early efficacy of Alkaline Phosphatase in sepsis patients with Renal Failure. | ||||||||||||||||||
Medical condition: Sepsis with Renal Failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003320-16 | Sponsor Protocol Number: CEL-03 | Start Date*: 2020-12-23 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:CeleCor Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3 prospective, blinded, randomized, placebo controlled, international multicenter study to assess the safety and efficacy of a single subcutaneous injection of zalunfiban in subjects with S... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Subjects with documented STEMI, presenting with persistent ischemic chest pain (>10 minutes) and new ≥2 mm ST-segment elevation in 2 adjacent ECG leads, in whom the total duration of symptoms to di... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) FR (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000712-33 | Sponsor Protocol Number: 2008/001 | Start Date*: 2008-05-13 | |||||||||||
Sponsor Name:Medizinische Universität Graz | |||||||||||||
Full Title: Fentanyl for the treatment of dsypnea in patients with chronic heart failure | |||||||||||||
Medical condition: Symptomatic treatment of dyspnea induced by chronic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001495-11 | Sponsor Protocol Number: BAMI-01 | Start Date*: 2013-05-06 |
Sponsor Name:Queen Mary University London | ||
Full Title: The effect of intracoronary reinfusion of bone marrow-derived mononuclear cells (BMMNC) on all causemortality in acute myocardial infarction | ||
Medical condition: Myocardial Infarction with reduced Left Ventricular ejection fraction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DK (Completed) GB (Completed) ES (Completed) IT (Completed) CZ (Completed) FI (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002671-14 | Sponsor Protocol Number: CRAD001ADE14 | Start Date*: 2008-02-18 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 15-month, multi-center, randomized, open-label, parallel group study investigating the renal tolerability, efficacy and safety of a CNI-free regimen (Certican® and MPA) versus a low-dose CNI- reg... | |||||||||||||
Medical condition: heart transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004656-30 | Sponsor Protocol Number: ICOR-2016-05 | Start Date*: 2018-10-19 | |||||||||||
Sponsor Name:Instituto de Investigación en Ciencias de la Salud Germans Trias i Pujol (IGTP) | |||||||||||||
Full Title: EVOlocumab in stable Heart Failure with reduced ejection fraction of ischemic etiology: EVO-HF Pilot | |||||||||||||
Medical condition: stable coronary artery disease and stable heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013713-99 | Sponsor Protocol Number: 2009.559 | Start Date*: 2010-04-14 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Does Cyclosporine ImpRove Clinical oUtcome in ST elevation myocardial infarction patients (CIRCUS study) | |||||||||||||
Medical condition: acute myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002154-20 | Sponsor Protocol Number: CLCZ696G2301 | Start Date*: 2017-03-28 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, active-controlled, parallel-group Phase 3 study to evaluate the efficacy and safety of LCZ696 compared to ramipril on morbidity and mortality in high risk ... | |||||||||||||
Medical condition: Left ventricular dysfunction following an acute myocardial infarction. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) GR (Completed) AT (Completed) SK (Completed) NL (Completed) ES (Completed) HU (Completed) BE (Completed) DK (Completed) SE (Completed) FI (Completed) BG (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003105-25 | Sponsor Protocol Number: MiLe-1 | Start Date*: 2014-08-27 |
Sponsor Name:Sahlgrenska University Hospital / The Queen Silvia Children´s Hospital | ||
Full Title: The prophylactic effect of levosimendan in reducing acute kidney injury postoperatively in pediatric patients undergoing corrective heart surgery | ||
Medical condition: Acute kidney injury postoperatively in connection with surgery for congenital heart disease | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-006072-32 | Sponsor Protocol Number: 2019/ABM/01/00078 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:University Hospital in Poznań | |||||||||||||
Full Title: Pulmonary REsistance modification under treatment with Sacubitil/valsartaN in paTients with HeartFailure with reduced ejection fraction | |||||||||||||
Medical condition: Heart Failure with reduced ejection fraction. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014769-16 | Sponsor Protocol Number: FO001 | Start Date*: 2010-06-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA` GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: REWORD-HF REverse WOrsening Renal function in Decompensated Heart Failure Impact of different therapeutic approaches in patients with cardiorenal syndrome in the setting of acute decompensated c... | |||||||||||||
Medical condition: acute decompensated congestive 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: 2005-003413-32 | Sponsor Protocol Number: CRAD001A2310 | Start Date*: 2006-01-31 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 24-month, multicenter, randomized, open-label non-inferiority study of efficacy and safety comparing two exposures of concentration-controlled Certican with reduced Neoral versus 3.0g MMF with st... | ||
Medical condition: de novo heart transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) DE (Completed) IT (Completed) DK (Prematurely Ended) BE (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005933-34 | Sponsor Protocol Number: SFHI01 | Start Date*: 2021-08-09 | |||||||||||
Sponsor Name:Sorin CRM SAS (Microport CRM) | |||||||||||||
Full Title: Evaluation of a modified Anti-Platelet Therapy associated with low-dose rapamycin DES Firehawk in Acute Myocardial Infarction Patients treated with complete revascularization strategy | |||||||||||||
Medical condition: Patients with clinically stable, low to moderate complexity acute Myocardial Infarction (MI; troponine-positive Non-ST-Elevation MI or ST-Elevation MI) requiring primary Percutaneous Coronary Inte... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) NL (Trial now transitioned) ES (Ongoing) IT (Ongoing) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005618-32 | Sponsor Protocol Number: 2021-HJEPharma-002 | Start Date*: 2022-06-29 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||||||||||||
Full Title: Dexamethasone, olanzapine, flow-targeted versus pressure-targeted hemodynamic management, and low tidal volume ventilation in patients undergoing on-pump cardiac surgery – a multifactorial design r... | |||||||||||||||||||||||
Medical condition: We investigate the efficacy of two pharmaceutical interventions for reducing mortality and organ damage, and shortening length of hospital stay in patients undergoing heart surgery (i.e. coronary a... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023211-34 | Sponsor Protocol Number: | Start Date*: 2011-04-27 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: Randomized Controlled Trial Comparing Intracoronary Administration of Adenosine or Sodium Nitroprusside to Control for Attenuation of Microvascular Obstruction During Primary Percutaneous Coronary ... | ||||||||||||||||||
Medical condition: Acute ST-segment Elevation Myocardial Infarction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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