- Trials with a EudraCT protocol (237)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
237 result(s) found for: Percutaneous coronary intervention.
Displaying page 9 of 12.
EudraCT Number: 2009-016178-33 | Sponsor Protocol Number: 1245.25 | Start Date*: 2010-11-12 | |||||||||||
Sponsor Name:Boehringer Ingelheim B.V. | |||||||||||||
Full Title: A Phase III, multicentre, international, randomised, parallel group, double blind cardiovascular safety study of BI 10773 (10 mg and 25 mg administered orally once daily) compared to usual care in ... | |||||||||||||
Medical condition: The study will be performed in patients with type 2 diabetes mellitus and high cardiovascular risk who have insufficient glycaemic control despite diet and exercise and are either treatment naïve o... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) ES (Completed) BE (Completed) FR (Completed) IT (Completed) HU (Completed) PT (Completed) GB (Completed) AT (Completed) GR (Completed) PL (Completed) EE (Completed) CZ (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: 2011-000480-27 | Sponsor Protocol Number: UCC-IGF-001 | Start Date*: 2011-06-03 | |||||||||||
Sponsor Name:University College Cork | |||||||||||||
Full Title: A Randomised Trial Evaluating the Safety and Efficacy of a Single Low Dose of Intracoronary Insulin-like Growth Factor-1 Following Percutaneous Coronary Intervention for ST-Elevation Acute Myocardi... | |||||||||||||
Medical condition: ST Elevation Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004997-41 | Sponsor Protocol Number: H7T-MC-TACW | Start Date*: Information not available in EudraCT |
Sponsor Name:Eli Lilly and Company | ||
Full Title: Effectiveness of Prasugrel versus Clopidogrel in Subjects with High Platelet Reactivity on Clopidogrel Following Elective Percutaneous Coronary Intervention with Implantation of Drug-Eluting Stent | ||
Medical condition: Reduction of composite cardio-vascular end-point in patients who have successfully undergone elective percutaneous coronary intervention with placement of at least one drug-eluting stent. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-003941-34 | Sponsor Protocol Number: 22021980 | Start Date*: 2008-02-11 |
Sponsor Name:Vorstand des Klinikums der Universität München - Grosshadern | ||
Full Title: SAFETY AND EFFICACY OF SITAGLIPTIN PLUS GRANULOCYTE-COLONY STIMULATING FACTOR IN PATIENTS SUFFERING FROM ACUTE MYOCARDIAL INFARCTION - SITAGRAMI-Trial | ||
Medical condition: Patients undergoing routine percutaneous coronary revascularisation for acute ST segment elevation myocardial infarction (STEMI, time from onset of infarction to intervention 2 to 24 hours) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002511-26 | Sponsor Protocol Number: 08062019 | Start Date*: 2019-12-20 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Repeated Injection Therapy of Allogeneic Stem Cells in Ischemic No-option Patients - A Multi-Centre Study (SCIENCE REPEAT) | |||||||||||||
Medical condition: Ischemic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010608-27 | Sponsor Protocol Number: ANG692 | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:MUMC+ | |||||||||||||
Full Title: A prospective cohort study to investigate the use of alfa V beta 3 integrin scintigraphic imaging with 99mTC-NC100692 to predict scar formation and heart failure after myocardial infarction in pati... | |||||||||||||
Medical condition: Myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019013-13 | Sponsor Protocol Number: IOP-116 | Start Date*: 2010-10-28 | ||||||||||||||||
Sponsor Name:BRACCO IMAGING | ||||||||||||||||||
Full Title: A Phase IV Pilot Study to Evaluate Kidney Damage Measured by Neutrophil Gelatinase- Associated Lipocalin (NGAL) as a New Bio-Marker in Patients with Normal eGFR Undergoing Percutaneous Coronary I... | ||||||||||||||||||
Medical condition: patients that are scheduled to undergo PCI with normal kidney function. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002312-27 | Sponsor Protocol Number: 13-031 | Start Date*: 2013-08-14 | ||||||||||||||||
Sponsor Name:Zealand Pharma | ||||||||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Parallel-Group Trial to Assess Clinical Efficacy and Safety of Danegaptide in Patients with ST-Elevation Myocardial Infarction undergoing Primary Per... | ||||||||||||||||||
Medical condition: The treatment of acute myocardial infarction, AMI is aimed at enabling the return of blood flow to the ischemic myocardium, thereby limiting the size of the infarct. However the reperfusion by itse... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-005172-17 | Sponsor Protocol Number: CHARITE-WKD-2005-1 | Start Date*: 2005-09-09 |
Sponsor Name:Charité/Campus Virchow-Klinikum, Medizinische Klinik m. S. Kardiologie | ||
Full Title: Renal haemodynamics during application of contrast media in patients undergoing cardiac catheterisation with high risk of acute renal failure: randomized comparison of different contrast media | ||
Medical condition: Patients with allready existing chronic renal failure undergoing a cardiac catheterisation for clinical reasons may develope an acute renal failure due to radio contrast media. This trial compares... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001876-32 | Sponsor Protocol Number: SLN360-002 | Start Date*: 2023-04-14 | ||||||||||||||||
Sponsor Name:Silence Therapeutics plc | ||||||||||||||||||
Full Title: A multi-centre, randomised, double-blind placebo-controlled, Phase 2 study to investigate efficacy, safety and tolerability of SLN360 in participants with elevated lipoprotein(a) at high risk of at... | ||||||||||||||||||
Medical condition: elevated lipoprotein (a) and high risk of atherosclerotic cardiovascular disease (ASCVD) events | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) NL (Completed) SK (Completed) DK (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003688-23 | Sponsor Protocol Number: 20180109 | Start Date*: 2020-10-13 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled Phase 2 Study to Evaluate Efficacy, Safety, and Tolerability of AMG 890 (a GalNAc-conjugated Small Interfering RNA [siRNA]) in Subjects with Elevated ... | |||||||||||||
Medical condition: Cardiovascular Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NL (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005149-18 | Sponsor Protocol Number: 033 | Start Date*: 2021-04-26 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Preclinical antiplatelet treatment with Cangrelor in patients presenting with ST-Elevation myocardial infarction: a randomized, double-blind, placebo-controlled pilot trial | ||
Medical condition: ST-Elevation Myocardial Infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
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: 2016-004501-14 | Sponsor Protocol Number: EDC-3135 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ZOLL, Inc. | |||||||||||||
Full Title: COOL-AMI EU PIVOTAL TRIAL: A MULTICENTER, PROSPECTIVE, RANDOMIZED- CONTROLLED TRIAL TO ASSESS THE SAFETY AND EFFECTIVENESS OF COOLING AS AN ADJUNCTIVE THERAPY TO PERCUTANEOUS INTERVENTION INP A TIE... | |||||||||||||
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: 2020-004455-32 | Sponsor Protocol Number: IMB101-006 | Start Date*: 2021-02-16 |
Sponsor Name:Imbria Pharmaceuticals, Inc. | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Exploratory Study on the Safety, Tolerability, and Pharmacodynamics of IMB-1018972 in Patients with Angina due to Coronary Syndrome | ||
Medical condition: Stable coronary artery disease (CAD) /Chronic coronary syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004626-17 | Sponsor Protocol Number: 1101/08 | Start Date*: 2009-03-23 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Anti-inflammatory and Anti-platelet effect of Clopidogrel and Aspirin vs Aspirin alone in Symptomatic Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
Medical condition: Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014986-22 | Sponsor Protocol Number: NC25113 | Start Date*: 2009-11-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized double blind, placebo-controlled clinical trial to assess the effects of taspoglutide (RO5073031) on cardiovascular outcomes in subjects with inadequately controlled type 2 diabetes an... | |||||||||||||
Medical condition: Patients with Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) HU (Prematurely Ended) EE (Prematurely Ended) CZ (Prematurely Ended) DE (Completed) SK (Prematurely Ended) ES (Completed) DK (Completed) BG (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000774-46 | Sponsor Protocol Number: BOOST-2 | Start Date*: 2005-08-18 |
Sponsor Name:Medical School, Dept. of Cardiology and Angiology | ||
Full Title: BOne marrOw transfer to enhance ST-elevation infarct regeneration-2 | ||
Medical condition: Patients with coronary artery disease, suffering from a large myocardial infarction. The loss of viable myocardium initiates a process of adverse left ventricular (LV) remodeling leading to chambe... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000846-42 | Sponsor Protocol Number: BY2015 | Start Date*: 2015-07-24 | |||||||||||
Sponsor Name:Stockholm South General Hospital | |||||||||||||
Full Title: Effects on re-endothelialisation with Bydureon treatment add on to Insulin versus Insulin alone, both in combination with Metformin in type 2 diabetic subjects (Rebuild Study). | |||||||||||||
Medical condition: Re-endothelialisation in type 2 diabetic subjects after Percutaneous coronary intervention (PCI) and stent placement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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