- Trials with a EudraCT protocol (108)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
108 result(s) found for: Sudden death.
Displaying page 1 of 6.
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: 2011-004984-55 | Sponsor Protocol Number: Nutri-Vita-D001 | Start Date*: 2012-05-04 | |||||||||||
Sponsor Name:SOCIETA' ITALIANA DI NEFROLOGIA | |||||||||||||
Full Title: Controlled randomised interventional trial on the use of 25-OH D vitamin in haemodialysis patients. | |||||||||||||
Medical condition: chronic haemodialysis patients | |||||||||||||
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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: 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: 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: 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: 2004-004260-71 | Sponsor Protocol Number: 1.1 | Start Date*: 2005-09-15 |
Sponsor Name:Medizinische Universität Wien Univ.Klinik f.Innere Medizin I/Hämatologie | ||
Full Title: Aspirin after six months or one year of oral anticoagulants for the prevention of recurrent venous thromboembolism and cardiovascular events in patients with idiopathic venous thromboembolism. The ... | ||
Medical condition: Venous thromboembolism, which includes deep vein thrombosis and pulmonary embolism. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004495-13 | Sponsor Protocol Number: BAY 59-7939/11702 | Start Date*: 2007-03-12 |
Sponsor Name:Bayer Healthcare AG | ||
Full Title: Oral direct factor Xa inhibitor rivaroxaban in patients with acute symptomatic deep-vein thrombosis or pulmonary embolism. | ||
Medical condition: Treatment and secondary prevention of venous thromboembolism in patients with acute symptomatic deep- vein thrombosis or pulmonary embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Completed) SE (Completed) FR (Completed) DE (Completed) FI (Completed) DK (Completed) HU (Completed) AT (Completed) IT (Completed) GB (Completed) CZ (Completed) NL (Completed) IE (Completed) LT (Completed) EE (Completed) LV (Completed) SK (Completed) | ||
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: 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: 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: 2007-000860-25 | Sponsor Protocol Number: CSPP100E2337 | Start Date*: 2007-07-27 |
Sponsor Name:Novartis Farmacéutica, SA | ||
Full Title: Estudio aleatorizado, doble ciego, controlado con placebo, de grupos paralelos, para determinar si la adición de Aliskiren al tratamiento convencional, en pacientes con diabetes tipo 2 y alto riesg... | ||
Medical condition: Diabetes tipo 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) PT (Prematurely Ended) FR (Completed) FI (Completed) GR (Completed) DE (Completed) DK (Completed) GB (Completed) LT (Completed) BE (Prematurely Ended) HU (Prematurely Ended) NL (Completed) AT (Completed) SE (Prematurely Ended) CZ (Completed) IT (Completed) SK (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: 2016-002019-16 | Sponsor Protocol Number: U-2015-030 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:Uppsala Clinical Research center | |||||||||||||
Full Title: Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure with Preserved Ejection Fraction | |||||||||||||
Medical condition: Heart Failure with Preserved Ejection Fraction, HFPEF | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002522-12 | Sponsor Protocol Number: P121001 | Start Date*: 2014-12-10 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux de Paris (AP-HP) | |||||||||||||
Full Title: European phase-II clinical trial evaluating efficacy of low dose rhIL-2 in patients with recently diagnosed type 1 diabetes | |||||||||||||
Medical condition: type -I diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2008-008412-47 | Sponsor Protocol Number: DRI10936 | Start Date*: 2009-09-21 | |||||||||||
Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Double blind placebo controlled dose ranging study of the efficacy and safety of celivarone at 50, 100 or 300 mg OD with Amiodarone as calibrator for the prevention of ICD interventions or death. | |||||||||||||
Medical condition: Ventricular arrhythmia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) HU (Completed) ES (Completed) PT (Completed) BE (Completed) SE (Completed) NL (Completed) IT (Completed) PL (Completed) FI (Completed) CZ (Completed) DK (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004212-21 | Sponsor Protocol Number: AMAG-423-201 | Start Date*: 2019-05-24 | |||||||||||
Sponsor Name:AMAG Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2b/3a, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of the Efficacy and Safety of AMAG-423, a Digoxin Immune Fab, in Antepartum Subjects with Severe Pree... | |||||||||||||
Medical condition: Severe Preeclampsia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) BE (Completed) RO (Completed) | |||||||||||||
Trial results: (No results available) |
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