- Trials with a EudraCT protocol (607)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
607 result(s) found for: End artery.
Displaying page 1 of 31.
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: 2021-006295-17 | Sponsor Protocol Number: MedTrace-002 | Start Date*: 2022-04-08 | |||||||||||
Sponsor Name:MedTrace Pharma | |||||||||||||
Full Title: A Phase 3, Multicenter, Open Label Study to Confirm the Diagnostic Potential of Intravenously Administered 15O- H2O to Identify Coronary Artery Disease During Pharmacological Stress and Resting Con... | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2004-004862-33 | Sponsor Protocol Number: BCBe/04/Neb-Gla/081 | Start Date*: 2006-05-23 |
Sponsor Name:Berlin-Chemie Menarini | ||
Full Title: INFLUENCE OF NEBIVOLOL ON OCULAR PERFUSION IN PATIENTS WITH ARTERIAL HYPERTENSION AND GLAUCOMA A mono-center, active-substance controlled, randomized, double-blind, prospective phase IV parallel-g... | ||
Medical condition: Arterial hypertension and glaucoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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: 2007-006263-68 | Sponsor Protocol Number: GEIDENo.A01207 | Start Date*: 2008-07-24 | |||||||||||
Sponsor Name:Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen | |||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF 6 MONTHS VERSUS 12 MONTHS CLOPIDOGREL THERAPY AFTER IMPLANTATION OF A DRUG-ELUTING STENT SAFETY AND EFFICACY OF SIX MONTHS DUAL ANTIPLATELET ... | |||||||||||||
Medical condition: Patients with established coronary artery disease on chronic clopidogrel therapy at 6 months after coronary drug eluting stent implantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006141-16 | Sponsor Protocol Number: OXBIO | Start Date*: 2006-10-13 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A Randomised, Placebo-Controlled Study of Two Doses of Oral 6R-BH4 on Vascular Function in Subjects with Coronary Artery Disease | |||||||||||||
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: 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: 2014-002171-29 | Sponsor Protocol Number: GE-IDE-MucT001-14 | Start Date*: 2015-07-16 | ||||||||||||||||
Sponsor Name:Hospital of the University of Munich, Grosshadern | ||||||||||||||||||
Full Title: Intensified Loading with Prasugrel versus Moderate Loading with Clopidogrel in PCI-treated Patients with Biomarker-Negative Angina pectoris. | ||||||||||||||||||
Medical condition: Biomarker-negative patients with an indication for percutaneous coronary intervention | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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: 2009-014690-41 | Sponsor Protocol Number: 0908033 | Start Date*: 2009-10-09 | |||||||||||||||||||||||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||||||||||||||||||||||
Full Title: Comparison of the protective effect of two cardioplegic solutions Custodiol versus St Thomas on the cardiac metabolism assessed by microdialysis in coronary surgery | |||||||||||||||||||||||||||||||||
Medical condition: Coronary surgery | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002343-30 | Sponsor Protocol Number: NEWTON-CABG | Start Date*: 2021-09-21 | |||||||||||
Sponsor Name:Unity Health Toronto, at its St. Michael’s site | |||||||||||||
Full Title: A randomized trial of evolocumab on saphenous vein graft patency following coronary artery bypass surgery (NEWTON-CABG) | |||||||||||||
Medical condition: Patency of graft after coronary bypass graft surgery in patients with hyprelipidaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003332-36 | Sponsor Protocol Number: ID-076A201 | Start Date*: 2017-12-20 | |||||||||||
Sponsor Name:Idorsia Pharmaceuticals Ltd. | |||||||||||||
Full Title: A multi-center, double-blind, randomized, placebo-controlled study to assess the pharmacodynamics, pharmacokinetics, tolerability, and safety of a single subcutaneous injection of ACT-246475 in adu... | |||||||||||||
Medical condition: stable coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Completed) SE (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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 (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002288-32 | Sponsor Protocol Number: ESR-14-10310 | Start Date*: 2016-11-14 | |||||||||||
Sponsor Name:Greek Corporation of Invasive Cardiology | |||||||||||||
Full Title: Ticagrelor Potentiation of Remote Ischemic Preconditioning: The Ticagrelor in Remote Ischemic Preconditioning (TRIP) study | |||||||||||||
Medical condition: Patient with NSTE-ACS referred for coronary angiography | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2020-005600-19 | Sponsor Protocol Number: APHP200072 | Start Date*: 2022-06-17 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: LEvOsimendaN vs. Placebo Before Tricuspid VAlve Surgery in Patients with Right Ventricular Dysfunction | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2023-000135-76 | Sponsor Protocol Number: ACE-01-22 | Start Date*: 2023-05-15 | |||||||||||||||||||||
Sponsor Name:Adamed Pharma S.A. | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence Study of Twice Daily Acetylsalicylic Acid Tablets 50 mg Compared to Once Daily Acetylsalicylic Acid Tablets 100 mg in Adult Patients Coronary Artery Disease (CAD) or Symptom... | |||||||||||||||||||||||
Medical condition: Coronary Artery Disease (CAD) or Symptomatic Peripheral Artery Disease (PAD) or after Acute Coronary Syndrome (ACS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (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 |
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