- Trials with a EudraCT protocol (190)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
190 result(s) found for: Left coronary artery.
Displaying page 1 of 10.
EudraCT Number: 2004-001959-11 | Sponsor Protocol Number: CL3-16257-056 | Start Date*: 2005-04-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales | |||||||||||||
Full Title: Effects of ivabradine on cardiovascular events in patients with stable coronary artery disease and left ventricular systolic dysfunction. A three-year randomised double-blind placebo-controlled int... | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) FI (Completed) LV (Completed) IT (Completed) CZ (Completed) SK (Completed) GB (Completed) DK (Completed) AT (Completed) SE (Completed) EE (Completed) DE (Completed) IE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023552-90 | Sponsor Protocol Number: BQ123CPBP2010 | Start Date*: 2011-05-05 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Abteilung für Herzchirurgie | ||||||||||||||||||||||||||||||||||||||
Full Title: Short-term endothelin A receptor blockade in patients with on-pump coronary artery bypass grafting | ||||||||||||||||||||||||||||||||||||||
Medical condition: aorto-coronary bypass surgery in patients with coronary artery disease | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006241-15 | Sponsor Protocol Number: GLUTAMICS2 | Start Date*: 2012-02-15 | |||||||||||
Sponsor Name:Linköping University Hospital | |||||||||||||
Full Title: GLUTAmate for Metabolic Intervention in Coronary Surgery II | |||||||||||||
Medical condition: Angina CCS class IV treated with coronary artery bypass surgery Coronary artery disease with moderate to severe left ventricular dysfunction treated with coronary artery bypass surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001945-42 | Sponsor Protocol Number: CRLX030A2203 | Start Date*: 2013-09-26 | |||||||||||
Sponsor Name:Novartis Pharma Service AG | |||||||||||||
Full Title: A multicenter, double blind, randomized, parallel group, placebo-controlled study to evaluate the effects of intravenous serelaxin infusion on micro- and macrovascular function in patients with cor... | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017725-19 | Sponsor Protocol Number: NC22703 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A Phase IIIB multicenter, double-blind, randomized, placebocontrolled study, evaluating the effect of treatment with dalcetrapib 600 mg on Atherosclerotic Disease as measured by I. Coronary Intrava... | |||||||||||||
Medical condition: A Study of the Effect of Dalcetrapib on Artherosclerotic Disease in Patients With Coronary Artery Disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012206-39 | Sponsor Protocol Number: ALX-0081-2.1/09 | Start Date*: 2009-08-14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Ablynx | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase II randomized, open label clinical trial in high risk percutaneous coronary intervention (PCI) patients receiving standard antithrombotic treatment plus either ALX-0081 or GPIIb/IIIa inhibi... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Thrombotic events associated with percutaneous coronary intervention (PCI) in patients with unstable angina or Non ST-Segment Elevation Myocardial Infarction (NSTEMI), or stable angina with at leas... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) AT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000998-68 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-07-02 | ||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Abteilung für Anästhesie und Intensivmedizin | ||||||||||||||||||
Full Title: Advanced antibiotic prophylaxis for optimal perioperative protection during coronary artery bypass grafting | ||||||||||||||||||
Medical condition: antibiotic prophylaxis during cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003492-39 | Sponsor Protocol Number: BR1-125 | Start Date*: 2008-04-29 | |||||||||||
Sponsor Name:Bracco Imaging S.p.A. | |||||||||||||
Full Title: A phase III study to compare SonoVue® enhanced myocardial echocardiography (MCE) to single photon emission computerized tomography (ECG-GATED SPECT), at rest and at peak of low-dose Dipyridamole s... | |||||||||||||
Medical condition: Suspected coronary artery disease (CAD) indicated for stress ECG-gated SPECT and coronary angiography to clarify whether they have a clinical significant coronary stenosis (=70%). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) NL (Completed) GB (Completed) IT (Completed) ES (Completed) GR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019352-42 | Sponsor Protocol Number: R09246M | Start Date*: 2010-08-19 | |||||||||||
Sponsor Name:Heart Center Co. Tampere University Hospital | |||||||||||||
Full Title: Effects of hypertonic saline-hydroxyethylstarch solution on extracellular water in cardiac surgery patients | |||||||||||||
Medical condition: Fifty adult male patients undergoing coronary bypass surgery will be enrolled in this study. Inclusion criteria are male gender and no need for pulmonary artery catheter (pulmonary hypertension or... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023839-42 | Sponsor Protocol Number: H8O-CY-O027 | Start Date*: 2011-04-29 | ||||||||||||||||
Sponsor Name:General University Hospital in Prague | ||||||||||||||||||
Full Title: EXEnatide in patients undergoing Coronary artery bypass grafting for improved glUcose conTrol and hemodynamIc ValuEs | ||||||||||||||||||
Medical condition: Patients with elective coronary artery bypass grafting with LV systolic dysfunction (EF LV ≤ 50%) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004601-47 | Sponsor Protocol Number: CKJX839D12303 | Start Date*: 2022-05-09 | |||||||||||
Sponsor Name:NOVARTIS PHARMA AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo controlled, parallelgroup Phase IIIb study evaluating the effect of inclisiran on atherosclerotic plaque progression assessed by coronary computed ... | |||||||||||||
Medical condition: Non-obstructive coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) IE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004881-16 | Sponsor Protocol Number: P05633 | Start Date*: 2009-06-10 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | |||||||||||||
Full Title: The Effect of Acadesine on Clinically Significant Adverse Cardiovascular and Cerebrovascular Events in High-Risk Subjects Undergoing Coronary Artery Bypass Graft (CABG) Surgery Using Cardiopulmonar... | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001148-40 | Sponsor Protocol Number: ExcelsiorLOAD | Start Date*: 2014-06-02 | |||||||||||||||||||||
Sponsor Name:Heart Center Freiburg - Bad Krozingen | |||||||||||||||||||||||
Full Title: Pharmacodynamic comparison of thienopyridine loading strategies in patients undergoing elective coronary stenting | |||||||||||||||||||||||
Medical condition: Stable patients with obstructive coronary heart disease undergoing elective percutaneous coronary stent implantation. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001962-25 | Sponsor Protocol Number: BR1-142 | Start Date*: 2016-03-04 | |||||||||||
Sponsor Name:Bracco Imaging S.p.A. | |||||||||||||
Full Title: A Prospective Multicenter Phase III Clinical Evaluation of the Safety and Efficacy of Lumason/SonoVue in Subjects Undergoing Pharmacologic Stress Echocardiography with Dobutamine for the Diagnosis ... | |||||||||||||
Medical condition: Suspected or known Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005071-25 | Sponsor Protocol Number: ExcelsiorLOAD2 | Start Date*: 2016-01-19 | |||||||||||||||||||||
Sponsor Name:University Heart Center Freiburg - Bad Krozingen | |||||||||||||||||||||||
Full Title: Pharmacodynamic comparison of different oral P2Y12-receptor inhibitor loading strategies for transitioning from cangrelor in patients undergoing coronary stenting | |||||||||||||||||||||||
Medical condition: Patients with obstructive coronary heart disease undergoing percutaneous coronary stent implantation. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016532-12 | Sponsor Protocol Number: Version1.0 | Start Date*: 2009-12-28 | ||||||||||||||||
Sponsor Name:Medical University of Vienna | ||||||||||||||||||
Full Title: Target tissue concentration of standard antibiotic treatment in coronary artery bypass grafting using left internal mammary artery | ||||||||||||||||||
Medical condition: antibiotic target tissue protection during cardiac surgery with the use of an internal mammary artery graft to prevent deep sternal wound infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020677-17 | Sponsor Protocol Number: ALMED-09-C3-026 | Start Date*: 2011-11-16 | |||||||||||
Sponsor Name:Air Liquide Santé International | |||||||||||||
Full Title: Efficacy and safety of xenon anaesthesia compared to sevoflurane anaesthesia and total intravenous anaesthesia for on-pump coronary artery bypass graft surgery: a randomised, three-arm, single-blin... | |||||||||||||
Medical condition: General anesthesia for on pump coronary artery bypass surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003260-37 | Sponsor Protocol Number: 1060 | Start Date*: 2015-10-22 | ||||||||||||||||||||||||||
Sponsor Name:Liverpool Heart and Chest Hospital | ||||||||||||||||||||||||||||
Full Title: Can Ivabradine attenuate post-revascularisation microcirculatory dysfunction in flow limiting coronary artery disease? | ||||||||||||||||||||||||||||
Medical condition: Coronary Artery Disease/Angina | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018175-14 | Sponsor Protocol Number: CL2-16257-088 | Start Date*: 2010-04-16 | ||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
Full Title: Effects of ivabradine IV versus placebo on haemodynamic parameters in patients with a low cardiac output syndrome following planned coronary artery bypass surgery and requiring positive inotropic t... | ||||||||||||||||||
Medical condition: Coronary Artery Disease patients presenting a low cardiac output syndrome following a planned coronary artery bypass graft and requiring a positive inotropic treatment with dobutamine administered ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001713-28 | Sponsor Protocol Number: BR1-141 | Start Date*: 2016-01-29 | |||||||||||
Sponsor Name:Bracco Imaging S.p.A. | |||||||||||||
Full Title: A Prospective Multicenter Phase III Clinical Evaluation of the Safety and Efficacy of Lumason™/SonoVue® in Subjects Undergoing Pharmacologic Stress Echocardiography with Dobutamine for the Diagnosi... | |||||||||||||
Medical condition: Suspected or known Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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