- Trials with a EudraCT protocol (241)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
241 result(s) found for: ST elevation myocardial infarction.
Displaying page 1 of 13.
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: 2006-006778-11 | Sponsor Protocol Number: BQ123AMI12/06 | Start Date*: 2007-04-26 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Internal Medicine II | |||||||||||||
Full Title: ENDOTHELIN RECEPTOR BLOCKADE IN ACUTE ST-ELEVATION MYOCARDIAL INFARCTION | |||||||||||||
Medical condition: Acute myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002709-36 | Sponsor Protocol Number: AK2017-3 | Start Date*: 2017-11-21 | ||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Physiology, Nuclear Medicine and PET | ||||||||||||||||||
Full Title: Phase II: 68Ga-NODAGA-E[c(RGDyK)]2 Angiogenese PET for imaging angiogenesis in ST-Elevation Myocardial Infarction(STEMI) | ||||||||||||||||||
Medical condition: ST-Elevation Myocardial Infarction (STEMI) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2020-004748-27 | Sponsor Protocol Number: EPIDAURUS-2020 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:LMU University Hospital Munich | |||||||||||||
Full Title: Escalated single platelet inhibition for one month plus direct oral anticoagulation in patients with atrial fibrillation and acute coronary syndrome undergoing percutaneous coronary intervention | |||||||||||||
Medical condition: Patients with atrial fibrillation and ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) (biomarker -positive acute coronary syndrome) und... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2007-002931-95 | Sponsor Protocol Number: LCC2010.01 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: The Effects of Nitric Oxide for Inhalation on Myocardial Infarction Size. | |||||||||||||
Medical condition: Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) HU (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: 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: 2005-005122-31 | Sponsor Protocol Number: CL2-16257-060 | Start Date*: 2006-04-25 | |||||||||||
Sponsor Name:Institut de Recherches Internationales (for France) [...] | |||||||||||||
Full Title: Evaluation of the effects on heart rate, haemodynamic parameters, safety and tolerability of 5 mg bolus of ivabradine followed by 8-hour infusion at the dose of 5 mg of ivabradine given after a per... | |||||||||||||
Medical condition: Acute Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023394-19 | Sponsor Protocol Number: 9129 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Maatschap Cardiologie Isala | |||||||||||||
Full Title: Early Beta blocker Administration before reperfusion in patients with ST-Elevation Myocardial Infarction who are planned to undergo primary PCI | |||||||||||||
Medical condition: Patients with acute ST elevation myocardial infarction, scheduled for emergency coronary angioplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003903-23 | Sponsor Protocol Number: P150946J | Start Date*: 2018-03-02 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Assessment of Beta blocker interruption after uncomplicated mYocardial infarction on Safety and Symptomatic cardiac events requiring hospitalization: The ABYSS Study | |||||||||||||
Medical condition: Myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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: 2022-003218-36 | Sponsor Protocol Number: 82646 | Start Date*: 2023-06-05 |
Sponsor Name:Radboudumc | ||
Full Title: The safety of ticagrelor monotherapy after primary percutaneous coronary intervention for ST-elevation myocardial infarction and the effect on intramyocardial haemorrhage | ||
Medical condition: Acute myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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: 2010-021277-36 | Sponsor Protocol Number: REGENERATE – AMI | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Queen Mary, University of London | |||||||||||||
Full Title: REGENERATE – AMI | |||||||||||||
Medical condition: Patients with acute ST-elevation myocardial infarction will be treated with progenitor cells after acute revascularisation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 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) |
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