- Trials with a EudraCT protocol (207)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    207 result(s) found for: ST segment elevation.
                    
                
			
   			
		
		Displaying page 1 of 11.
	
	
	| EudraCT Number: 2008-007290-20 | Sponsor Protocol Number: TMC-BIV-08-03 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:The Medicines Company UK Ltd. | ||||||||||||||||||
| Full Title: European Ambulance Acute Coronary Syndrome Angiox Trial: EUROMAX | ||||||||||||||||||
| Medical condition: Patients presenting with ST-Segment Elevation Acute Coronary Syndrome (STE-ACS) planned for a primary Percutaneous Coronary Intervention (PCI) management strategy | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) DK (Completed) FR (Completed) NL (Completed) CZ (Completed) ES (Completed) PL (Completed) IT (Completed) SI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-001325-34 | Sponsor Protocol Number: 17/2008/U/Sper | Start Date*: 2008-04-01 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: PROMISE AMI (PROtection of coronary Microcirculation by Iloprost: Safety and Efficacy evaluation in Acute Myocardial Infarction treated by primary PCI) Pilot Study | |||||||||||||
| Medical condition: Acute myocardial infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005369-64 | Sponsor Protocol Number: iBEAST/2 | Start Date*: 2015-06-19 | |||||||||||
| Sponsor Name:Consorci MAr Parc de Salut de Barcelona | |||||||||||||
| Full Title: Improve the myocardial reperfusion in ST elevation myocardial infarction: a randomized study between standard percutaneous coronary intervention with thrombectomy and pharmacological approach guide... | |||||||||||||
| Medical condition: ST elevation myocardial infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012120-89 | Sponsor Protocol Number: CARDIOTA80-2009 | Start Date*: 2009-09-23 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: 80MG ATORVASTATIN THERAPY IN PATIENTS WITH ST ELEVATION MYOCARDIAL INFARCTION TREATED WITH PRIMARY PTCA | |||||||||||||
| Medical condition: ST elevation Myocardial Infarct | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000303-42 | Sponsor Protocol Number: 9050 | Start Date*: 2006-09-25 | |||||||||||
| Sponsor Name:ISALA KLINIEKEN | |||||||||||||
| Full Title: A randomized, double blind controlled trial evaluating the benefits of early up-front-loaded high dose Tirofiban in the treatment of patients with ST-segment elevation myocardial infarction, who ar... | |||||||||||||
| Medical condition: acute myocardial infarction with ST segment elevation | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
| 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 | ||||||||||||||||||
| EudraCT Number: 2011-002876-18 | Sponsor Protocol Number: 2011-002876-18 | Start Date*: 2011-12-19 | |||||||||||
| Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
| Full Title: CYCLosporinE A in reperfused acute myocardial infarction (CYCLE-Trial) | |||||||||||||
| Medical condition: All (male and female) patients, aged over 18, presenting with a large STEMI not older than 4 hours (defined as angina pectoris or equivalent symptoms of more than 30 minutes duration within the las... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010295-23 | Sponsor Protocol Number: ARCARDIO002 | Start Date*: 2009-03-07 | |||||||||||
| Sponsor Name:AZIENDA USL 8 AREZZO | |||||||||||||
| Full Title: Load & Go trial: Safety and effectiveness of three different clopidogrel loading doses, administered at first medical contact in patients with acute myocardial infarction undergoing primary angiopl... | |||||||||||||
| 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: 2014-004238-25 | Sponsor Protocol Number: 2012-004-0402-CARD | Start Date*: 2015-02-09 | |||||||||||||||||||||
| Sponsor Name:The Royal Wolverhampton NHS Trust | |||||||||||||||||||||||
| Full Title: Pharmacokinetics and Pharmacodynamics of Platelet P2Y12 Inhibitors in Patients Undergoing Percutaneous Coronary Intervention (PCI) for Acute Myocardial Infarction: A Pilot Study | |||||||||||||||||||||||
| Medical condition: ST-segment elevation myocardial infarction Non ST-segment elevation myocardial infarction | |||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-001642-26 | Sponsor Protocol Number: LRD.2016.STREAM2 | Start Date*: 2017-10-02 | |||||||||||
| Sponsor Name:Leuven Research & Development (LRD) at University of Leuven, Belgium | |||||||||||||
| Full Title: STREAM-2 (STrategic Reperfusion in elderly patients Early After Myocardial Infarction) | |||||||||||||
| Medical condition: ST-elevation myocardial infarction within 3 hours of onset of symptoms | |||||||||||||
					
						
							
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-002547-25 | Sponsor Protocol Number: ARC1779-003 | Start Date*: 2007-12-19 | ||||||||||||||||
| Sponsor Name:Archemix Corp. | ||||||||||||||||||
| Full Title: A Phase 2 Study of an Aptameric von Willebrand Factor Antagonist, ARC1779, in Patients with Acute Myocardial Infarction Undergoing Percutaneous Coronary Intervention | ||||||||||||||||||
| Medical condition: ACS Patients with Acute Myocardial Infarction Undergoing Percutaneous Coronary Intervention (ST segemnt elevation MI and Non ST segemtn elevation MI) | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-003721-41 | Sponsor Protocol Number: SKS-CANTI2016 | Start Date*: 2018-03-01 | |||||||||||
| Sponsor Name:Department of Cardiology, Aarhus University Hospital, Skejby | |||||||||||||
| Full Title: Cangrelor versus Ticagrelor for Early Platelet Inhibition in ST-Elevation Myocardial Infarction. (The CanTi study) | |||||||||||||
| Medical condition: ST-elevation Myocardial Infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000313-38 | Sponsor Protocol Number: EFC5965 | Start Date*: 2007-01-24 | |||||||||||
| Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: Randomized, multinational, double-blind study, comparing a high loading dose regimen of clopidogrel versus standard dose in patients with unstable angina or myocardial infarction managed with an ea... | |||||||||||||
| Medical condition: Patients with non-ST segment elevation myocardial infarction managed with an early PCI. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) FI (Completed) IE (Completed) SK (Completed) FR (Completed) SE (Completed) DE (Completed) AT (Completed) EE (Completed) BG (Completed) GR (Completed) IT (Completed) GB (Completed) LT (Completed) NL (Completed) LV (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001924-16 | Sponsor Protocol Number: FDY-5301-302 | Start Date*: 2022-04-13 | |||||||||||
| Sponsor Name:Faraday Pharmaceuticals, Inc. | |||||||||||||
| Full Title: IOCYTE AMI-3: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Intravenous FDY-5301 in Patients with an Anterior ST-Elevation Myocardial Infarction | |||||||||||||
| Medical condition: Anterior ST-Elevation Myocardial Infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) SK (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) PT (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001883-31 | Sponsor Protocol Number: CARMRUSMIAMBULANCE20190823 | Start Date*: 2020-02-25 | 
| Sponsor Name:VU Univesity Medical Center (VUmc) | ||
| Full Title: Microvascular Recovery using contrast Ultrasound in ST-elevation Myocardial Infarction in the ambulance (MRUSMI-Ambulance) | ||
| Medical condition: ST elevation myocardial infarction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023779-24 | Sponsor Protocol Number: M10-1028 | Start Date*: 2010-12-06 | 
| Sponsor Name:Stichting Toegepast Caridologisch Onderzoek | ||
| Full Title: A Comparison of Drug Eluting and Bare Metal Stents with Bivalirudin during PCI or Bivalirudin for 4 hours in Acute Coronary Syndromes. The Eindhoven Reperfusion Study | ||
| Medical condition: Patients with ACS who are scheduled for primary PCI (STEMI) or for immediate PCI < 2.5 hours or early PCI < 48 hours (NSTEMI) and who are pre-treated with HLD clopidogrel | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-001219-44 | Sponsor Protocol Number: 1123.28 | Start Date*: 2008-01-30 | |||||||||||
| Sponsor Name:Boehringer Ingelheim France | |||||||||||||
| Full Title: STREAM - STrategic Reperfusion Early After Myocardial Infarction Comparison of the efficacy and safety of a strategy of pre-hospital fibrinolytic treatment with tenecteplase and additional antipla... | |||||||||||||
| Medical condition: ST-elevation myocardial infaction within 3 hours of onset of symptoms | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) AT (Completed) GB (Completed) IT (Completed) ES (Completed) BE (Completed) DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002824-42 | Sponsor Protocol Number: SPIRI-201 | Start Date*: 2012-04-17 | |||||||||||
| Sponsor Name:Stealth Peptides Inc. | |||||||||||||
| Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety, Tolerability and Efficacy of Intravenous Bendavia™ (MTP-131) on Reperfusion Injury in Patients Treated with St... | |||||||||||||
| Medical condition: Reperfusion injury in ST-segment Elevation Myocardial Infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007676-42 | Sponsor Protocol Number: P071101 | Start Date*: 2008-04-07 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude ATOLL . Etude internationale, multicentrique, visant à comparer l'utilisation de l'enoxaparine IV versus héparine standard IV chez les sujets présentant un infarctus du myocarde aigu et néces... | |||||||||||||
| Medical condition: infarctus aigu du myocarde avec élévation du segment ST sur le point de subir une intervention coronaire percutanée (ICP) | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003340-24 | Sponsor Protocol Number: APHP210015 | Start Date*: 2021-12-21 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Rituximab in patients with ST-elevation myocardial infarction. A phase 2 placebo-controlled randomized clinical trial | |||||||||||||
| Medical condition: ST-elevation myocardial infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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