- Trials with a EudraCT protocol (51)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
51 result(s) found for: Coronary sinus.
Displaying page 1 of 3.
EudraCT Number: 2012-004779-38 | Sponsor Protocol Number: CL3-16257-102 | Start Date*: 2013-04-16 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Effects of ivabradine on plaque burden, morphology and composition in patients with clinically indicated coronary angiography. A randomised double-blind placebo-controlled international multicentre... | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) PT (Prematurely Ended) SK (Prematurely Ended) BE (Prematurely Ended) DE (Completed) CZ (Completed) HU (Prematurely Ended) PL (Prematurely Ended) SE (Prematurely Ended) NO (Prematurely Ended) DK (Prematurely Ended) GR (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001989-15 | Sponsor Protocol Number: HomRate04_2012 | Start Date*: 2012-09-17 | |||||||||||
Sponsor Name:Universität des Saarlandes | |||||||||||||
Full Title: A randomised, placebo controlled, double blind, cross-over, single center clinical Study to investigate the effect of heart rate reduction with ivabradine on endothelial function and vascular stiff... | |||||||||||||
Medical condition: Stable coronary heart disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2007-003026-14 | Sponsor Protocol Number: PREVENTBURDEN | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:KA Rudolfstiftung - 2. Medizinische Abteilung | |||||||||||||
Full Title: | |||||||||||||
Medical condition: coronary artery disease with a single coronary vessel requiring stent implantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011360-10 | Sponsor Protocol Number: CL3-16257-083 | Start Date*: 2009-10-13 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Efectos de ivabradina en pacientes con arteriopatía coronaria estable sin insuficiencia cardíaca clínica. Estudio multicéntrico, internacional, aleatorizado, doble ciego, controlado con placebo St... | |||||||||||||
Medical condition: Arteriopatia Coronaria Estable Stable coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) GB (Completed) NL (Completed) FI (Completed) LV (Completed) HU (Completed) CZ (Completed) SK (Completed) IE (Completed) BE (Completed) FR (Completed) LT (Completed) DE (Completed) AT (Completed) SE (Completed) IT (Completed) GR (Completed) EE (Completed) SI (Completed) BG (Completed) DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000783-98 | Sponsor Protocol Number: CL2-16257-095 | Start Date*: 2011-09-26 | |||||||||||
Sponsor Name:INSTITUT DE RECHERCHES INTERNATIONALES SERVIER | |||||||||||||
Full Title: Effects of oral administration of ivabradine (7.5 mg bid) on post-ischaemic stunning induced by exercise stress in patients with coronary artery disease and exercise inducible ischaemia. | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001419-29 | Sponsor Protocol Number: HRVCTA1 | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Universitätsklinik für Radiodiagnostik | |||||||||||||
Full Title: Influence of iodinated contrast agents on heart rate variation and diagnostic image quality during CT angiography of the coronary arteries | |||||||||||||
Medical condition: CT angiography of the coronary arteries | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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: 2007-006793-28 | Sponsor Protocol Number: CL3-16257-078 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | |||||||||||||
Full Title: Effects of a 10 or 15 mg single intravenous bolus of ivabradine versus placebo on heart rate control during a multislice computed tomography coronary angiography for the evaluation of coronary arte... | |||||||||||||
Medical condition: Heart rate control during a MultiSlice Computed Tomography Coronary Angiography (MST CA) for the evaluation of Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) BE (Completed) PT (Completed) HU (Completed) ES (Completed) DE (Completed) FR (Completed) DK (Completed) IT (Completed) PL (Completed) BG (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: 2011-004779-35 | Sponsor Protocol Number: CL2-16257-096 | Start Date*: 2012-04-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Effects of oral chronic administration of ivabradine (7.5 mg bid) in comparison to placebo (bid) on top of beta-blockers, on central aortic blood pressure. Randomized, cross-over, double blind, mul... | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001788-37 | Sponsor Protocol Number: HCA-2015-2 | Start Date*: 2015-06-29 | ||||||||||||||||
Sponsor Name:Heart Center Co. Tampere University Hospital | ||||||||||||||||||
Full Title: Effects of volume changes to the plethysmography signal on major surgery patients | ||||||||||||||||||
Medical condition: Patients scheduled for elective CABG (Coronary artery bypass surgery). Patients scheduled for elective open major abdominal surgery (gastrointestinal surgery). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016914-25 | Sponsor Protocol Number: CEDRICStudie | Start Date*: 2011-08-08 |
Sponsor Name:Deutsches Herzzentrum Berlin | ||
Full Title: CEDRIC: Clopidogrel- Effects on Diameter Reduction and Intimal Hyperplasia in Long-term Follow up after Cardiac Transplantation | ||
Medical condition: Transplant vasculopathy after heart transplantation characterized by Stanford type B2 lesions in coronary angiography and by microvasculopathy proven in biopsy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004825-14 | Sponsor Protocol Number: D1680C00016 | Start Date*: 2016-05-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Investigate the Effects of Saxagliptin, Saxagliptin Combined with Dapagliflozin, and Sitagliptin in Pat... | |||||||||||||
Medical condition: Patients with type 2 diabetes mellitus and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) HU (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003638-17 | Sponsor Protocol Number: HEMOPURE II and/or COR-002 | Start Date*: 2005-10-28 |
Sponsor Name:Biopure Corporation | ||
Full Title: This is a phase II, open-label study in the catheterization laboratory setting to challenge the concept that HBOC-201 ® administration might improve myocardial ‘oxygenation’ and myocardial function... | ||
Medical condition: Treatment of several ischemic conditions, such as acute coronary syndromes (ACS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001430-18 | Sponsor Protocol Number: 5101127 | Start Date*: 2019-08-12 |
Sponsor Name:Kuopio University Hospital | ||
Full Title: Does postoperative intravenous corticosteroid and intravenous beta blocker management prevent atrial fibrillation after cardiac surgery? | ||
Medical condition: new onset atrial fibrillation and paroxysmal atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002643-10 | Sponsor Protocol Number: HCA-2011_1 | Start Date*: 2012-01-17 |
Sponsor Name:Heart Center Co. Tampere University Hospital | ||
Full Title: Intracoronary administration of levosimendan in cardiac surgery patients | ||
Medical condition: Dysfunction after opening of aortic cross-clamp in patients undergoing aortic valve and coronary artery bypass (AVR+CABG) operation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005715-32 | Sponsor Protocol Number: SOCODIHF | Start Date*: 2017-12-07 |
Sponsor Name:Karolinska Institutet Stockholm, Sweden | ||
Full Title: SOdium-glucose CO-transporter inhibition in patients with Type 2 Diabetes and Ischemic Heart Failure (SOCODIHF) | ||
Medical condition: Patients with type 2 diabetes mellitus and heart failure of ischemic origin | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-001452-11 | Sponsor Protocol Number: 201103 | Start Date*: 2011-06-07 |
Sponsor Name:Skånes Universitetssjukhus Lund | ||
Full Title: Supplemental Oxygen in Catherized Coronary Emergency Reperfusion | ||
Medical condition: Acute ST elevation myocardial infaction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000500-26 | Sponsor Protocol Number: 01-1-101 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Rapidscan Pharma Solutions EU Ltd (RPS EU Ltd) | |||||||||||||
Full Title: An Open-label, Single Ascending-dose, Pharmacokinetic and Safety Study of Regadenoson (Rapidscan®) in Paediatric Patients with Cardiovascular Conditions and Diseases | |||||||||||||
Medical condition: Regadenoson will be used as a pharmacologic stress agent in paediatric patients with cardiovascular problems, undergoing a clinically indicated myocardial perfusion MRI | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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