- Trials with a EudraCT protocol (530)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
530 result(s) found for: Acute Myocardial Infarction.
Displaying page 2 of 27.
| EudraCT Number: 2006-003819-45 | Sponsor Protocol Number: GE IDE No. I01106 | Start Date*: 2007-01-07 | |||||||||||
| Sponsor Name:Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München | |||||||||||||
| Full Title: PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF ERYTHROPOIETIN IN PATIENTS WITH ST-SEGMENT ELEVATION MYOCARDIAL INFARCTION UNDERGOING PERCUTANEOUS CORONARY INTERVENTION. REVIVAL-... | |||||||||||||
| Medical condition: Patients with ST-segment elevation myocardial infarction undergoing percutaneous coronary intervention. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002189-21 | Sponsor Protocol Number: 838/15 | Start Date*: 2015-07-10 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: "The combined effect of subcutaneous Granulocyte - Colony Stimulating Factor and Myocardial Contrast Echocardiography with intravenous infusion of sulphur hexafluoride on post-infarction left ventr... | |||||||||||||
| Medical condition: acute myocardial infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000054-35 | Sponsor Protocol Number: 2016-ECCLIPSESTEMI-01 | Start Date*: 2016-05-20 | |||||||||||
| Sponsor Name:Fundación Interhospitalaria Investigación Cardiovascular | |||||||||||||
| Full Title: Effects of Intravenous Lysine Acetylsalicylate versus Oral Aspirin on Platelet Responsiveness in Patients with ST-segment Elevation Myocardial Infarction: a Pharmacodynamic study (ECCLIPSE-STEMI tr... | |||||||||||||
| Medical condition: Myocardial Infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000211-33 | Sponsor Protocol Number: P02100 | Start Date*: 2016-10-06 | |||||||||||
| Sponsor Name:Papworth Hospital NHS Foundation Trust | |||||||||||||
| Full Title: Dose Effect Relationship of a Single Dose of Rituximab on the Kinetics of B Lymphocytes in Patients with Acute ST-Segment Myocardial Infarction | |||||||||||||
| Medical condition: Anterior STEMI revascularised by PPCI | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003458-26 | Sponsor Protocol Number: CSLCT-HDL-12-77 | Start Date*: 2014-07-15 | |||||||||||
| Sponsor Name:CSL Behring LLC | |||||||||||||
| Full Title: A Phase 2b, Multi-center, Randomized, Placebo-controlled, Dose-ranging Study to Investigate the Safety and Tolerability of Multiple Dose Administration of CSL112 in Subjects with Acute Myocardial I... | |||||||||||||
| Medical condition: Acute Myocardial Infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) IT (Completed) CZ (Completed) AT (Completed) DK (Completed) HU (Completed) NL (Completed) ES (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000619-51 | Sponsor Protocol Number: FX06AQ-II-01 | Start Date*: 2006-07-10 | |||||||||||
| Sponsor Name:Fibrex Medical Research & Development GmbH | |||||||||||||
| Full Title: A Multicenter, Double-blind, Randomized, Placebo-Controlled Study to Measure the Effect of FX06 (a fibrin derived peptide Bβ15-42) on Ischemia-Reperfusion Injury in Patients Undergoing Primary Perc... | |||||||||||||
| Medical condition: Patients with acute myocardial infarction (AMI) indicated for Percutaneous Coronary Intervention (PCI). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) DK (Completed) AT (Completed) NL (Completed) CZ (Completed) BE (Completed) LT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005259-32 | Sponsor Protocol Number: Eprotection/2007/05 | Start Date*: 2005-04-27 | |||||||||||
| Sponsor Name:Imperial College Heathcare NHS Trust | |||||||||||||
| Full Title: A phase 2 randomised trial to investigate the effects of recombinant human erythropoietin on infarct size in patients undergoing primary percutaneous coronary angiography for ST-segment elevation m... | |||||||||||||
| Medical condition: Acute ST elevation myocardial infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010869-23 | Sponsor Protocol Number: THIRST 02/2009 | Start Date*: 2009-06-22 | ||||||||||||||||||||||||||
| Sponsor Name:OSPEDALE G.PASQUINUCCI-FONDAZIONE TOSCANA GABRIELE MONASTERIO/CNR | ||||||||||||||||||||||||||||
| Full Title: Acute and long term effects of thyroid hormone replacement therapy in patients with ST-Elevation Myocardial Infarction (STEMI) and borderline/reduced triiodothyronine levels. | ||||||||||||||||||||||||||||
| Medical condition: All patients enrolled in the study should be in good clinical conditions, being ST-elevation myocardial infarction the main pathology,, without evidence of clinical/hemodynamic instability. All pat... | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-005140-16 | Sponsor Protocol Number: KAI-9803-004 | Start Date*: 2009-06-02 | |||||||||||
| Sponsor Name:KAI Pharmaceuticals, Inc | |||||||||||||
| Full Title: Inhibition of δ-PROTEin kinase C for the reducTION of infarct size in Acute Myocardial Infarction (PROTECTION AMI) | |||||||||||||
| Medical condition: Acute Myocardial Infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) ES (Completed) HU (Completed) CZ (Completed) PT (Completed) BE (Completed) SE (Completed) FI (Completed) IT (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002407-14 | Sponsor Protocol Number: 106915 | Start Date*: 2006-10-24 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research, European Medical Governance | |||||||||||||
| Full Title: Eptifibatide Versus Abciximab in primary PCI for Acute ST elevation Myocardial Infarction (EVA-AMI) | |||||||||||||
| Medical condition: Primary percutaneous coronary intervention (PCI) for ST-elevation Myocardial Infarction (STEMI) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014272-21 | Sponsor Protocol Number: IC2009exe001 | Start Date*: 2009-11-03 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Effect of additional treatment with exenatide in patients with an acute myocardial infarction: the EXAMI trial) | |||||||||||||
| Medical condition: Acute Myocardial Infartion to be treated with primary PCI | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-003701-27 | Sponsor Protocol Number: 07-113 | Start Date*: 2007-12-20 | |||||||||||
| Sponsor Name:Portola Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Randomized Trial to Evaluate the Effect of Adjunctive Antiplatelet Therapy with Intravenous PRT060128, a Selective P2Y12-Receptor Inhibitor, Before Primary Percutaneous Intervention in Patients w... | |||||||||||||
| Medical condition: Adjunctive antiplatelet therapy prior to primary percutaneous intervention in patients with ST-Elevation Myocardial Infarction (STEMI) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000142-20 | Sponsor Protocol Number: 2003056 | Start Date*: 2004-10-01 | |||||||||||
| Sponsor Name:Procter & Gamble Pharmaceuticals | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Parallel-group, Placebo-Controlled Study of Pexelizumab in Patients with Acute Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention | |||||||||||||
| Medical condition: Following as ST-wave elevation myocardial infarction, there is local ischemia. When reperfusion occurs, there is a complement mediated inflammatory reponse, known as reperfusion injury, and a syst... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) ES (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000334-30 | Sponsor Protocol Number: RON004 | Start Date*: 2015-05-28 | |||||||||||||||||||||||||||||||
| Sponsor Name:Professor Thomas John Kiernan | |||||||||||||||||||||||||||||||||
| Full Title: Peripheral endothelial function assessment of patients on ticagrelor versus clopidogrel who have undergone percutaneous coronary intervention - a randomized, crossover study | |||||||||||||||||||||||||||||||||
| Medical condition: Peripheral arterial vasoactivity in patients with coronary artery disease who have undergone percutaneous coronary intervention | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-004220-23 | Sponsor Protocol Number: VIDEAT | Start Date*: 2008-09-04 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: EFFECT OF SUPPLEMENTATION WITH CHOLECALCIFEROL ON GLUCOSE AND LIPID METABOLISM, BLOOD PRESSURE, BONE MASS, QUALITY OF LIFE, CARDIOVASCULAR MORBIDITY AND MORTALITY IN PATIENTS WITH ISCHAEMIC HEART D... | |||||||||||||
| Medical condition: ISCHAEMIC ARTERY DISEASE | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019461-29 | Sponsor Protocol Number: ETAMI | Start Date*: 2011-03-25 | |||||||||||
| Sponsor Name:Stiftung Institut für Herzinfarktforschung | |||||||||||||
| Full Title: ETAMI-Study: Early Thienopyridine treatment to improve primary PCI in Patients with Acute Myocardial Infarction | |||||||||||||
| Medical condition: Myocardial infarction <= 12 hours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014343-36 | Sponsor Protocol Number: GE IDE NO. I01209 | Start Date*: 2009-09-09 | |||||||||||
| Sponsor Name:Deutsches Herzzentrum | |||||||||||||
| Full Title: RANDOMIZED TRIAL OF PRASUGREL PLUS BIVALIRUDIN VERSUS CLOPIDOGREL PLUS HEPARIN IN PATIENTS WITH ACUTE STEMI BAVARIAN REPERFUSION ALTERNATIVES EVALUATION [BRAVE-4] TRIAL | |||||||||||||
| Medical condition: Acute myocardial infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000765-36 | Sponsor Protocol Number: ID-076A202 | Start Date*: 2018-06-22 | |||||||||||
| Sponsor Name:Idorsia Pharmaceuticals Ltd | |||||||||||||
| Full Title: A multi-center, open-label, randomized, study to assess the onset of platelet aggregation inhibition after a single subcutaneous injection of ACT-246475 in adults with acute myocardial infarction | |||||||||||||
| Medical condition: Acute myocardial infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-008491-13 | Sponsor Protocol Number: 2008-008491-13 | Start Date*: 2009-03-07 | ||||||||||||||||||||||||||
| Sponsor Name:AZIENDA USL 8 AREZZO | ||||||||||||||||||||||||||||
| Full Title: A Multicentric randomized comparison between iso-osmolar and ipo-osmolar contrast agents in STEMI patients undergoing primary PCI. Assessment of contrast-induced nephropathy incidence and myocardia... | ||||||||||||||||||||||||||||
| Medical condition: Patients with Acute Myocardial Infarction within 12 hours after the onset of symptoms | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-008936-10 | Sponsor Protocol Number: NIMINI-1/2 | Start Date*: 2009-03-16 | |||||||||||
| Sponsor Name:Division of Cardiology, Robert-Bosch-Krankenhaus | |||||||||||||
| Full Title: Comparative evaluation of different CMR pulse-sequences with respect to their practicability and diagnostic performance in diagnosing the inflamed myocardium in patients with acute myocardial infar... | |||||||||||||
| Medical condition: Patients with acute myocardial infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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