- Trials with a EudraCT protocol (357)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
357 result(s) found for: Coronary Heart Disease NOS.
Displaying page 3 of 18.
| EudraCT Number: 2021-006072-16 | Sponsor Protocol Number: AUMC25485 | Start Date*: 2022-08-09 | |||||||||||
| Sponsor Name:Amsterdam University Medical Center (AUMC) | |||||||||||||
| Full Title: Dual-AntiPlatelet Therapy strategies FOR elective PCI in a REAL-world setting | |||||||||||||
| Medical condition: Coronary artery disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001672-70 | Sponsor Protocol Number: 17.3.2008 | Start Date*: 2008-05-30 | ||||||||||||||||
| Sponsor Name:Heli Leppikangas | ||||||||||||||||||
| Full Title: The effects of levosimendan on haemodynamics in patients undergoing elective aortic valve replacement (AVR) together with coronary artery bypass grafting (CABG) surgry | ||||||||||||||||||
| Medical condition: Aortic valve dysfunction and coronary artery disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-002650-38 | Sponsor Protocol Number: Pre65 | Start Date*: 2008-07-01 | |||||||||||||||||||||
| Sponsor Name:Organisation name was not entered | |||||||||||||||||||||||
| Full Title: Vähentääkö pregabaliini opioidikipulääkityksen tarvetta ja kroonisen kivun esiintyvyyttä alle 65-vuotiailla potilailla sydänleikkauksen jälkeen? | |||||||||||||||||||||||
| Medical condition: Tutkimukseen otetaan potilaan suostumuksella alle 65-vuotiaita avosydänleikkauk-seen joko koronaariohitus- tai sydämen läppärekonstruktioon tulevia potilaita, jotka leikatataan perfuusioleikkauksena. | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2007-004000-13 | Sponsor Protocol Number: D356IC00001 | Start Date*: 2008-02-07 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: Study of Coronary Atheroma by InTravascular Ultrasound: Effect of Rosuvastatin Versus AtorvastatiN (SATURN): A 104-week, randomized, double-blind, parallel group, multi-center Phase IIIb study comp... | ||
| Medical condition: Coronary Atheroma -- The current trial will study patients who have a clinical indication for coronary catheterization and who have coronary artery disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) FR (Completed) IT (Completed) BE (Completed) HU (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004376-35 | Sponsor Protocol Number: ISSBRILO176 | Start Date*: 2014-01-14 | |||||||||||
| Sponsor Name:Hellenic Cardiovascular Research Society | |||||||||||||
| Full Title: A Single Center, Phase II, Assessor-Blinded, RaNdomized, Active Controlled, Parallel-Group Trial to COmpare Ticagrelor Versus Clopidogrel on the REduction of ArteriaL STiffness and Wave Reflections... | |||||||||||||
| Medical condition: Coronary Artery Disease (with an indication for coronary angiography) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007297-38 | Sponsor Protocol Number: 1483/08 | Start Date*: 2009-09-01 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Effects of Atorvastatin on Number and Function of Pro-inflammatory CD4+CD28null T-cells and Defective Treg in Patients with Acute Coronary Syndromes | |||||||||||||
| Medical condition: acute coronary syndrome without ST segment elevation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000296-15 | Sponsor Protocol Number: E5555-G000-202 | Start Date*: 2007-11-22 | |||||||||||
| Sponsor Name:Eisai Limited | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-Controlled Study of the Safety and Tolerability of E5555, and its Effects on Clinical Events and Biomarkers in Patients with Non-ST-Segment Elevation Acute Coron... | |||||||||||||
| Medical condition: Coronary Artery Disease | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) GB (Completed) BE (Completed) DE (Completed) NL (Completed) SE (Completed) CZ (Completed) PL (Completed) IE (Completed) IT (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000190-31 | Sponsor Protocol Number: MEDCOR2011 | Start Date*: 2011-05-27 | ||||||||||||||||
| Sponsor Name:Therabel Pharmaceuticals Ltd | ||||||||||||||||||
| Full Title: Double-blind parallel placebo-controlled study to evaluate the effect of Molsidomine on the Endothelial Dysfunction in patients with stable angina pectoris undergoing a percutaneous CORonary interv... | ||||||||||||||||||
| Medical condition: Patients with stable angina undergoing elective PCI, used an add-on treatment on standard care therapy, molsidomine or placebo to improve the endothelial function (12 months treatment) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: Removed from public view | ||||||||||||||||||
| EudraCT Number: 2015-005568-40 | Sponsor Protocol Number: LoDoCo2 | Start Date*: 2016-08-01 | |||||||||||
| Sponsor Name:Werkgroep Cardiologische centra Nederland | |||||||||||||
| Full Title: Low-dose colchicine for secondary prevention of cardiovascular disease | |||||||||||||
| Medical condition: cardiovascular disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000583-96 | Sponsor Protocol Number: 2011-000583-96 | Start Date*: 2011-08-05 | |||||||||||
| Sponsor Name:Aarhus University Hospital, Skejby | |||||||||||||
| Full Title: Undersøgelse af 6-uger versus 6-måneders clopidogrel behandling hos patienter med samtidig aspirin og oral angikoagulans behandling efter implantation af en drug-eluting stent | |||||||||||||
| Medical condition: Patients with coronary artery disease and ongoing treatment with an oral anticoagulant agent (warfarin), who have indication for treatment with a drug-eluting stent and therefore have indication fo... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000156-16 | Sponsor Protocol Number: A509 1043 | Start Date*: 2004-09-14 | |||||||||||
| Sponsor Name:Pfizer AB | |||||||||||||
| Full Title: Phase 3 multi center, double blind, randomized, parallel group evaluation of the fixed combination torcetrapib/atorvastatin, administered orally, once daily (QD), compared with atorvastatin alone, ... | |||||||||||||
| Medical condition: Coronary Heart Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) ES (Completed) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000334-30 | Sponsor Protocol Number: RON004 | Start Date*: 2015-05-28 | |||||||||||||||||||||||||||||||
| Sponsor Name:Professor Thomas John Kiernan | |||||||||||||||||||||||||||||||||
| Full Title: Peripheral endothelial function assessment of patients on ticagrelor versus clopidogrel who have undergone percutaneous coronary intervention - a randomized, crossover study | |||||||||||||||||||||||||||||||||
| Medical condition: Peripheral arterial vasoactivity in patients with coronary artery disease who have undergone percutaneous coronary intervention | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-000504-18 | Sponsor Protocol Number: A01711 | Start Date*: 2011-05-10 | ||||||||||||||||||||||||||
| Sponsor Name:Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen | ||||||||||||||||||||||||||||
| Full Title: DABI-ADP-2: IMPACT OF DABIGATRAN AND PHENPROCOUMON ON CLOPIDOGREL MEDIATED ADP INDUCED PLATELET AGGREGATION IN PATIENTS WITH ATRIAL FIBRILLATION | ||||||||||||||||||||||||||||
| Medical condition: Patients with atrial fibrillation and in indication for oral anticoagulation, who are currently receiving additionally clopidogrel for another medical condition, such as acute coronary syndrome and... | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2012-001668-31 | Sponsor Protocol Number: CL3-16257-097 | Start Date*: 2012-10-05 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Safety of oral chronic administration of ivabradine modified release formulation compared to ivabradine immediate release formulation, in patients with stable coronary artery disease. A 6 to 12-mon... | |||||||||||||
| Medical condition: Stable coronary artery disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) HU (Completed) DE (Completed) SK (Completed) NL (Completed) ES (Completed) BG (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005070-31 | Sponsor Protocol Number: CHUBX 2007/19 | Start Date*: 2007-12-04 | ||||||||||||||||
| Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
| Full Title: Analyse prospective des pontages et valves aortiques sous anticoagulation conventionnelle versus hemi-dose en système clos et coa | ||||||||||||||||||
| Medical condition: Cardiopahtie / Valvulopathie | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-004424-20 | Sponsor Protocol Number: 36319968 | Start Date*: 2007-11-05 | |||||||||||
| Sponsor Name:Helsinki Uniersity Central Hospital | |||||||||||||
| Full Title: HES 130/0.4 vaikutus hyytymisjärjestelmään off-pump-sepelvaltimokirurgian jälkeen | |||||||||||||
| Medical condition: Sepelvaltimotauti I20.0 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002519-22 | Sponsor Protocol Number: Atorvastatina-CD34 | Start Date*: 2007-05-30 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: Endothelial progenitor cells mobilization induced by atorvastatin in patients with chronic coronaric disease (stable angina) treated with revascularization with antibody antiCD34 covered stent | |||||||||||||
| Medical condition: coronaric chronic disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000388-18 | Sponsor Protocol Number: DIAS-001-FFR | Start Date*: 2016-03-24 | |||||||||||
| Sponsor Name:Diasolve Ltd | |||||||||||||
| Full Title: A randomised crossover investigation to evaluate and compare the effectiveness, safety and feasibility of a novel dedicated Over-The-Wire FFR Infusion MicroCatheter (HYPEREM IC) for measuring fract... | |||||||||||||
| Medical condition: This is a single‐blind, randomised, crossover investigation comparing the investigational device using intra‐coronary (IC) Adenosine infusion to the standard intravenous (IV) infusion method used f... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004064-29 | Sponsor Protocol Number: CS747S-B-U4003 | Start Date*: 2012-06-11 | |||||||||||
| Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
| Full Title: A PHARMACODYNAMIC EVALUATION OF SWITCHING FROM TICAGRELOR TO PRASUGREL IN SUBJECTS WITH STABLE CORONARY ARTERY DISEASE: 2ND SWITCHING ANTIPLATELET AGENTS (SWAP 2) | |||||||||||||
| Medical condition: Stable Coronary Artery Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001094-58 | Sponsor Protocol Number: BAY 59-7939 / 15572 | Start Date*: 2011-09-13 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: Prospective, multi-center, randomized, heparin-controlled dose-finding trial to evaluate the efficacy and safety of rivaroxaban, a direct factor Xa inhibitor, on the background of standard dual ant... | |||||||||||||
| Medical condition: Symptomatic CAD patients due to undergo an elective (non emergent) Percutaneous Coronary Intervention (PCI) on one or two lesions in the native coronary vessel(s). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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