- Trials with a EudraCT protocol (185)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
185 result(s) found for: Sinus rhythm.
Displaying page 1 of 10.
EudraCT Number: 2008-001201-42 | Sponsor Protocol Number: 4-001-LVS | Start Date*: 2008-06-01 | |||||||||||
Sponsor Name:POLICLINICO SAN DONATO IRCSS | |||||||||||||
Full Title: Clinical trial on the use of ivabradine in patients with inappropriate sinus tachycardia | |||||||||||||
Medical condition: Inappropriate sinus tachycardia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003789-15 | Sponsor Protocol Number: 9.2 | Start Date*: 2019-12-17 |
Sponsor Name:Department of Cardiology, Hartcentrum, University Medical Center Groningen | ||
Full Title: Digoxin Evaluation in Chronic heart failure: Investigational Study In Outpatients in the Netherlands | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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: 2015-001529-18 | Sponsor Protocol Number: LGN-VN-003 | Start Date*: 2015-08-18 |
Sponsor Name:Laguna Pharmaceuticals, Inc. | ||
Full Title: RESTORE SR: A multi-center, Randomized, double-blind, placebo-controlled study to Evaluate the Safety and efficacy of a single oral dose of vanoxerine for The conversion Of subjects with REcent ons... | ||
Medical condition: Recent atrial fibrillation (AF) or atrial flutter (AFL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) NL (Ongoing) PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005525-48 | Sponsor Protocol Number: AK-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Diakonhjemmet hospital | ||
Full Title: Potassium infusion for conversion of atrial fibrillation/atrial flutter. | ||
Medical condition: Atrial fibrillation / atrial flutter | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001898-90 | Sponsor Protocol Number: Crijns01.12-02-026 | Start Date*: 2012-06-25 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Effects of vernakalant and flecainide on atrial contractility in patients with atrial fibrillation | ||
Medical condition: Patients with paroxysmal or persistent atrial fibrillation (AF) reporting at the first heart aid. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004102-90 | Sponsor Protocol Number: 3628 | Start Date*: 2007-05-25 |
Sponsor Name:Oxford Radcliffe Hospitals NHS Trust | ||
Full Title: Efficacy and safety of amiodarone 100mg versus 200mg for the maintenance of sinus rhythm after cardioversion of atrial fibrillation | ||
Medical condition: Atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004865-11 | Sponsor Protocol Number: IV-FLEC | Start Date*: 2022-03-21 |
Sponsor Name:Win Medica Pharmaceuticals S.A. | ||
Full Title: Comparison of the effectiveness of IntraVenous FLECainide plus oral ranolazine versus intravenous flecainide alone in the cardioversion of recent onset atrial fibrillation – a randomized, prospecti... | ||
Medical condition: Restoration of sinus rhythm in patients with recent AF onset | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002516-33 | Sponsor Protocol Number: NCT01420393 | Start Date*: 2015-09-03 |
Sponsor Name:University of Ottawa Heart Institute | ||
Full Title: A Randomized Ablation-based atrial Fibrillation rhythm control versus rate control Trial in patients with heart failure and high burden Atrial Fibrillation | ||
Medical condition: The study is comparing two accepted treatment methods (rhythm control-Catheter ablation with or without anti-arrhythmic drug control of maintaining sinus rhythm versus rate controls with medical th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000695-34 | Sponsor Protocol Number: Verna-Ibu-AF_1.0 | Start Date*: 2011-07-22 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.-Klinik für Notfallmedizin | |||||||||||||
Full Title: Vernakalant Versus Ibutilide In Recent-Onset Atrial Fibrillation | |||||||||||||
Medical condition: recent-onset atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001354-25 | Sponsor Protocol Number: | Start Date*: 2005-07-26 |
Sponsor Name:University of Dundee | ||
Full Title: Use of Omega-3 poyunsaturated Fatty Acid Supplements to Maintain Sinus Rhythm in Persistent Atrial Fibrillation:a prospective and randomised study. | ||
Medical condition: Patients with persistent atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-023101-35 | Sponsor Protocol Number: CJI-202 | Start Date*: 2011-02-11 | |||||||||||
Sponsor Name:Sequel Pharmaceuticals Inc. | |||||||||||||
Full Title: TUNDRA-AF: A mulTi-center, randomized, doUble-bliNded, placebo-controlled Dose-escalating study of the effects of K201 on the RestorAtion of sinus rhythm in subjects with symptomatic Atrial Fibri... | |||||||||||||
Medical condition: Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000833-38 | Sponsor Protocol Number: ISIS329993-CS6 | Start Date*: 2012-06-19 | |||||||||||
Sponsor Name:Isis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2 Study to Assess the Antiarrhythmic and Symptomatic Effect of the Second Generation Antisense Oligonucleotide ISIS 329993 Targeting CRP in Patients with Paroxysmal Atrial Fibrillation | |||||||||||||
Medical condition: Atrial fibrillation (AF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000346-21 | Sponsor Protocol Number: S219.3.118 | Start Date*: 2004-11-05 |
Sponsor Name:Solvay Pharmaceuticals GmbH | ||
Full Title: Controlled, Parallel Design Study to Evaluate the Efficacy and Safety of Intravenous Tedisamil Sesquifumarate in the Rapid Conversion to Normal Sinus Rhythm in Female Subjects with Recent Onset Atr... | ||
Medical condition: Recent Onset Atrial Fibrillation or Flutter | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: HU (Completed) ES (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001129-17 | Sponsor Protocol Number: LDLL300.301 | Start Date*: 2017-06-19 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals GmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: A multicenter, open-label study to investigate the effectiveness and safety of AOP Landiolol in controlling supraventricular tachycardia in pediatric patients (LANDI-PED). | ||||||||||||||||||||||||||||||||||||||
Medical condition: Supraventricular tachycardia in pediatric patients. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) DE (Ongoing) LT (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001384-11 | Sponsor Protocol Number: captaf | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Catheter Ablation compared with Pharmacological Therapy for Atrial Fibrillation – the CAPTAF trial | |||||||||||||
Medical condition: To study the effect of catheter ablation (using CE marked products) on the quality of life an in patients with atrial fibrillation depsite treatment with conevntional antiarrhythmic medical therapy... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002262-37 | Sponsor Protocol Number: ATP1 | Start Date*: 2004-10-27 |
Sponsor Name:Newcastle Hospitals Trust | ||
Full Title: Adenosine testing in the diagnosis of unexplained syncope: A pilot study | ||
Medical condition: Syncope | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001260-29 | Sponsor Protocol Number: 2012-CARDAF | Start Date*: 2012-04-24 | |||||||||||
Sponsor Name:FONDAZIONE ISTITUTO SAN RAFFAELE-G.GIGLIO | |||||||||||||
Full Title: Identification of predictive plasma Biomarkers and use of a high dosage statin during a procedure of Parrossistic Atrial Fibrillation pharmacological Cardioversion | |||||||||||||
Medical condition: Parossistic Atrial Fibrillation according to the European Socierty of Cardiology (ESC)criteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001766-40 | Sponsor Protocol Number: DRI5165 | Start Date*: 2004-12-20 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Recherche | |||||||||||||
Full Title: Placebo controlled double blind dose ranging study of the efficacy and safety of SSR149744C 50, 100, 200, or 300 mg OD, with amiodarone as calibrator for the maintenance of sinus rhythm in patients... | |||||||||||||
Medical condition: Atrial fibrillation/flutter | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SE (Completed) DK (Completed) IT (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001716-59 | Sponsor Protocol Number: D4120C00002 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multi-Centre, Double-Blind, Randomised, Placebo-Controlled Phase II Study to Assess the Effects on Atrial and Ventricular Refractoriness of an Intravenous Infusion of AZD2927 in Patients Undergoi... | |||||||||||||
Medical condition: Arrhythmia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: View results |
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