- Trials with a EudraCT protocol (139)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
139 result(s) found for: ST Elevation Myocardial Infarction (STEMI).
Displaying page 7 of 7.
EudraCT Number: 2009-012852-26 | Sponsor Protocol Number: EFC11319 | Start Date*: 2010-09-06 | |||||||||||
Sponsor Name:sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Estudio multicéntrico doble ciego, aleatorizado, controlado con placebo y de grupos paralelos, para evaluar los eventos cardiovasculares durante el tratamiento con lixisenatide en pacientes con dia... | |||||||||||||
Medical condition: Diabetes tipo II ___________________ Type II Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) PT (Completed) GB (Completed) LT (Completed) EE (Completed) DK (Completed) LV (Completed) IT (Completed) NL (Completed) SE (Completed) FR (Completed) FI (Completed) BG (Completed) BE (Completed) NO (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001277-14 | Sponsor Protocol Number: P01910 | Start Date*: 2016-02-19 | ||||||||||||||||
Sponsor Name:Royal Papworth Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: A Randomised Mechanistic Study Comparing the Effects of Different Anti-platelet Combinations (Ticagrelor vs. Placebo/ Clopidogrel) with Aspirin in Patients presenting with STEMI Treated with Primar... | ||||||||||||||||||
Medical condition: Patients with ST segment 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: 2011-000911-26 | Sponsor Protocol Number: Uni-Koeln-1392 | Start Date*: 2011-05-12 |
Sponsor Name:University of Cologne | ||
Full Title: Heart rate control after acute myocardial infarct | ||
Medical condition: successful percutaneous intervention in patients with acute ST-elevated myocardial infarct | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001069-18 | Sponsor Protocol Number: 12/0533 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:University College London (UCL) | |||||||||||||
Full Title: MINeralocorticoid receptor antagonist pretreatment to MINIMISE reperfusion injury after ST-Elevation Myocardial Infarction(STEMI). | |||||||||||||
Medical condition: Cardiovascular disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001534-19 | Sponsor Protocol Number: APHP200015 | Start Date*: 2021-05-21 |
Sponsor Name:AP-HP/DRCI | ||
Full Title: Direct oral Anticoagulants for Prevention of lEft ventRIcular Thrombus after anterior acute myocardial InFarction | ||
Medical condition: Left ventricular (LV) thrombus after acute myocardial infarction (AMI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000339-24 | Sponsor Protocol Number: APOLLO_01 | Start Date*: 2007-12-18 |
Sponsor Name:Cytori Therapeutics, Inc | ||
Full Title: A randomized clinical trial of AdiPOse-derived stem ceLLs in the treatment of patients with ST elevation myOcardial infarction – The APOLLO Trial | ||
Medical condition: patients with ST-elevation myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) ES (Completed) | ||
Trial results: Removed from public view |
EudraCT Number: 2012-003423-37 | Sponsor Protocol Number: PRIME | Start Date*: 2012-07-31 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Prospective randomized study ARMYDA PRIME | |||||||||||||
Medical condition: patients with acute myocardial infarction with ST elevation (STEMI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013498-17 | Sponsor Protocol Number: IC ClearLy | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Cardiologia - Azienda Ospedaliero Universitaria di Modena | |||||||||||||
Full Title: IntraCoronary Abciximab with the ClearWay Catheter To Improve Outcomes with Lysis (IC ClearLy) Trial | |||||||||||||
Medical condition: The study will enroll male or female ACS patients at least 18 years of age presenting with STEMI with angiographically visible thrombus (Thrombus Grade >2) who are planned to undergo emergency PCI ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000631-27 | Sponsor Protocol Number: NCT01778842 | Start Date*: 2014-01-28 | ||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||||||||||||||||||
Full Title: PhaRmacodynamic Effect of antiplatelet agents in elderly patients: Standard clopidogrel versus prasugrEl low dose Therapy. | ||||||||||||||||||
Medical condition: Patients over 75 years with acute coronary syndrome | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000671-17 | Sponsor Protocol Number: 3163 K1-200-WW | Start Date*: 2005-10-05 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., Clinical Research and Development | ||
Full Title: A Safety and Efficacy Dose-Ranging Study of GAP-486 in Subjects With Nonsustained Ventricular Tachycardia and Acute Ischemia | ||
Medical condition: Subjects with coronary artery disease or left ventricular dysfunction experiencing an acute coronary syndrome with non-life-threatening ventricular arrhythmias. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) DK (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002628-29 | Sponsor Protocol Number: R&D6327 | Start Date*: 2014-09-09 |
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Evaluating the effectiveness of intravenous ciclosporin on reducing reperfusion injury in patients undergoing primary percutaneous coronary intervention: a double-blind, phase II, randomised contro... | ||
Medical condition: Myocardial ischemia/reperfusion injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001772-38 | Sponsor Protocol Number: G112 | Start Date*: 2013-06-29 | |||||||||||
Sponsor Name:A.N.M.C.O.-Fondazione Italiana lotta Malattie Cardiovasc | |||||||||||||
Full Title: STEM-AMI OUTCOME TRIAL STem cElls Mobilization in Acute Myocardial Infarction Outcome Trial | |||||||||||||
Medical condition: Patients with left ventricular systolic disfunction after revascularization for acute myocardial infarction | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002892-34 | Sponsor Protocol Number: D3560L00052 | Start Date*: 2005-10-28 |
Sponsor Name:AstraZeneca SAS | ||
Full Title: Comparison of the Effects Noted in The ApoB/ApoA-I ratio Using Rosuvastatin and atorvastatin in patients with acUte coronary Syndrome. | ||
Medical condition: Men or women who are >18 and <75 years old diagnosed with non ST elevation - acute coronary syndrome (NSTE-ACS) and onset of clinical symptoms less than 24 hours at the admission for which a PCI is... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) ES (Completed) PT (Completed) EE (Completed) HU (Completed) IT (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001358-81 | Sponsor Protocol Number: CTPX01 | Start Date*: 2014-05-20 |
Sponsor Name:Coretherapix S.L.U. | ||
Full Title: "First-in-human clinical trial, double blind, randomized with placebo, open for the six first patients (dose ranging), to evaluate the safety and efficacy of intracoronary infusion of allogeneic hu... | ||
Medical condition: Acute Myocardial Infarction (AMI): "First STEMI submitted to elective primary PCI with successful revascularization by PCI (TIMI = 3), but intermediate-high risk of HF development (infarct size by... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000485-29 | Sponsor Protocol Number: STH19752 | Start Date*: 2017-05-23 |
Sponsor Name:Dr | ||
Full Title: Prolonged ENoxapariN in primarY Percutaneous Coronary Intervention; a Pilot Pharmacodynamic study (PENNY PCI study) | ||
Medical condition: ST elevation myocardial infarction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021591-28 | Sponsor Protocol Number: TMC-CAN-10-01 | Start Date*: 2011-01-05 | |||||||||||
Sponsor Name:The Medicines Company | |||||||||||||
Full Title: A clinical trial comparing cangrelor to clopidogrel standard of care therapy in subjects who require percutaneous coronary intervention | |||||||||||||
Medical condition: Subjects with coronary atheroschlerosis who require PCI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) IT (Completed) DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002876-26 | Sponsor Protocol Number: 2017-002876-26 | Start Date*: 2018-10-19 | |||||||||||
Sponsor Name:South Tees Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Telomerase ACTivator to reverse Immunosenescence in Acute Coronary Syndrome: a double-blind, phase II, pilot randomised controlled trial (TACTIC) | |||||||||||||
Medical condition: Immunosenescence in patients who have had an acute coronary syndrome diagnosed within the last 6 months. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003935-56 | Sponsor Protocol Number: TMC-CAN-05-03 | Start Date*: 2006-11-24 | |||||||||||
Sponsor Name:The Medicines Company | |||||||||||||
Full Title: A clinical trial comparing treatment with cangrelor (in combination with usual care) to usual care, in subjects who require percutaneous coronary intervention | |||||||||||||
Medical condition: Subjects with coronary atherosclerosis (excluding ST segment-elevation MI [STEMI]) who require PCI (with or without stent). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Completed) CZ (Prematurely Ended) LT (Completed) SK (Completed) DE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000192-14 | Sponsor Protocol Number: TMC-CAN-05-02 | Start Date*: 2006-12-21 | |||||||||||
Sponsor Name:The Medicines Company | |||||||||||||
Full Title: A Clinical Trial Comparing Cangrelor To Clopidogrel In Subjects Who Require Percutaneous Coronary Intervention | |||||||||||||
Medical condition: Subjects with coronary atherosclerosis who require PCI (with or without stent). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Completed) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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