- Trials with a EudraCT protocol (71)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
71 result(s) found for: Sudden cardiac death.
Displaying page 1 of 4.
EudraCT Number: 2016-004277-41 | Sponsor Protocol Number: 16.0012 | Start Date*: 2017-01-18 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:St George's University of London | ||||||||||||||||||||||||||||||||||||||
Full Title: An observational study into the variety of electrocardiographic responses to an ajmaline Provocation in healthy subjects. What are the genetic and structural variations dictating this response ? | ||||||||||||||||||||||||||||||||||||||
Medical condition: Study in the healthy population. This is a study of a test used in the diagnosis of the condition, Brugada Syndrome. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002386-37 | Sponsor Protocol Number: IVN3ICD | Start Date*: 2007-08-24 |
Sponsor Name:Department of Cardiology, Aalborg Hospital | ||
Full Title: Intravenous infusion of n-3 polyunsaturated fatty acids and ventricular tackycardi in patients with implantable cardioverter defibrillator (ICD) | ||
Medical condition: Patients with an implantable cardioverter defibrillator (ICD-unit) for treatment for cardiac ventricular arrhythmias and for prevention of sudden cardiac death | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
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: 2009-010236-18 | Sponsor Protocol Number: CSPP100A2368 | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos, controlado con placebo para evaluar la eficacia y seguridad a 6 meses de la terapia de aliskiren, además de la terapia estánda... | |||||||||||||
Medical condition: Insuficiencia Cardiaca aguda descompensada | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) CZ (Completed) BE (Completed) IT (Completed) SK (Completed) PL (Completed) HU (Completed) SE (Completed) FI (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001006-34 | Sponsor Protocol Number: 2015C104 | Start Date*: 2016-10-25 |
Sponsor Name:University Medical Centre Groningen (UMCG) | ||
Full Title: Groningen Intervention study for the Preservation of cardiac function with sodium thiosulfate after ST-segment elevation myocardial infarction | ||
Medical condition: ST-segment elevated myocardial infarction, decompensatio cordis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001117-13 | Sponsor Protocol Number: C3BS-C-11-01 | Start Date*: 2012-11-14 | |||||||||||
Sponsor Name:Celyad SA | |||||||||||||
Full Title: Efficacy and Safety of Bone Marrow-Derived Mesenchymal Cardiopoietic Cells (C3BS-CQR-1) for the Treatment of Chronic Advanced Ischemic Heart Failure | |||||||||||||
Medical condition: Chronic advanced symptomatic heart failure secondary to ischemic cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) HU (Completed) PL (Completed) SE (Completed) ES (Completed) IE (Completed) BG (Completed) LT (Completed) EE (Prematurely Ended) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011291-29 | Sponsor Protocol Number: RACE 3 | Start Date*: 2011-08-16 | |||||||||||
Sponsor Name:Interuniversity Cardiology Institute of the Netherlands (ICIN) | |||||||||||||
Full Title: Routine versus Aggressive Upstream Rhythm Control for Prevention of Early Atrial Fibrillation in Heart Failure: RACE 3 | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001679-22 | Sponsor Protocol Number: EMPA-UMCG-1 | Start Date*: 2017-10-27 | |||||||||||||||||||||
Sponsor Name:Univeristy Medical Center Groningen | |||||||||||||||||||||||
Full Title: Randomized, double blind, placebo controlled, multicenter pilot study on the effects of empagliflozin on clinical outcomes in patients with acute decompensated heart failure | |||||||||||||||||||||||
Medical condition: Acute (decompensated) heart failure | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004954-33 | Sponsor Protocol Number: 7U/2014 | Start Date*: 2014-11-27 | |||||||||||
Sponsor Name:Central Finland Hospital District | |||||||||||||
Full Title: Medical ANtiarrhythmic Treatment or Radiofrequency Ablation in ischemic Ventricular Tachyarrhythmias. A prospective, randomized multicentre study MANTRA-VT | |||||||||||||
Medical condition: Ventricular tachyarrhtyhmias in patients with prior myocardial infarction and implantable cardioverter defibrillator | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000994-39 | Sponsor Protocol Number: BRD 06/2-D | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Nantes | |||||||||||||
Full Title: Evaluation de l'intérêt d'un traitement par hydroquinidine pour la prise en charge des patients atteints d'un syndrome de Brugada à risque rythmique élevé et implantés d'un défibrillateur | |||||||||||||
Medical condition: Patients with syndroma of Brugada who have an automatic implantable cardiac defibrillator | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001191-19 | Sponsor Protocol Number: 2011-400 | Start Date*: 2011-10-26 | |||||||||||
Sponsor Name:Hjertemedicinsk klinik B, 2142, Rigshospitalet | |||||||||||||
Full Title: Cardiac effects of inhibition of the renin angiotensin system with losartan in patients with hypertrophic cardiomyopathy. | |||||||||||||
Medical condition: Hypertrophic cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004505-16 | Sponsor Protocol Number: CONVINCE | Start Date*: 2016-08-08 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:University College Dublin | ||||||||||||||||||||||||||||||||||||||
Full Title: CONVINCE - (COlchicine for preventioN of Vascular Inflammation in Non- CardioEmbolic stroke) – a randomised clinical trial of low-dose colchicine for secondary prevention after stroke | ||||||||||||||||||||||||||||||||||||||
Medical condition: The prevention of recurrent stroke and coronary events (fatal and non- fatal) after ischaemic stroke and transient ischaemic attack (TIA) not caused by cardiac embolism or other causes unrelated to... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) DE (Completed) CZ (Completed) DK (Completed) PT (Completed) BE (Completed) LT (Completed) NL (Completed) | ||||||||||||||||||||||||||||||||||||||
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) |
EudraCT Number: 2015-003895-65 | Sponsor Protocol Number: DAL-301 | Start Date*: 2016-06-22 | |||||||||||
Sponsor Name:DalCor Pharma UK Ltd, Leatherhead, Swiss Branch Zug | |||||||||||||
Full Title: A phase III, double-blind, randomized placebo-controlled study to evaluate the effects of dalcetrapib on cardiovascular (CV) risk in a genetically defined population with a recent Acute Coronary Sy... | |||||||||||||
Medical condition: This study is investigating the cardiovascular morbidity and mortality (cardiovascular death, resuscitated cardiac arrest, non-fatal myocardial infarction (MI) and non-fatal stroke) in subjects wit... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) SE (Completed) SK (Completed) DK (Completed) FI (Completed) PT (Completed) DE (Completed) HU (Completed) ES (Ongoing) AT (Completed) CZ (Completed) BG (Completed) RO (Ongoing) PL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2022-001604-17 | Sponsor Protocol Number: APHP220428 | Start Date*: 2022-11-15 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux de Paris | |||||||||||||
Full Title: Effect of Short-Term Prednisone Therapy on C-Reactive Protein Change in Emergency Department Patients With Acute Heart Failure and Elevated Inflammatory Markers | |||||||||||||
Medical condition: Patients With Acute Heart Failure and Elevated Inflammatory Markers in Emergency Department | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
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: 2018-000916-75 | Sponsor Protocol Number: REC-DUT-002 | Start Date*: 2018-06-07 |
Sponsor Name:RECARDIO Inc. | ||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study of Dutogliptin in Combination with Filgrastim in Early Recovery Post-Myocardial Infarction | ||
Medical condition: Acute myocardial infarction, acute myocardial ischemia, STEMI ST elevation myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) AT (Prematurely Ended) BE (Completed) NL (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) | ||
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: 2015-005568-40 | Sponsor Protocol Number: LoDoCo2 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:Werkgroep Cardiologische centra Nederland | |||||||||||||
Full Title: Low-dose colchicine for secondary prevention of cardiovascular disease | |||||||||||||
Medical condition: cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
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