- Trials with a EudraCT protocol (106)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
106 result(s) found for: Artery wall.
Displaying page 1 of 6.
EudraCT Number: 2008-003839-20 | Sponsor Protocol Number: CVT5127 | Start Date*: 2009-02-24 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Open-Label, Parallel-Group, Exploratory Study to Evaluate the Efficacy and Safety of 400 µg Regadenoson Bolus for Pharmacological Stress Echocardiography | |||||||||||||
Medical condition: Suspected coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2012-001427-12 | Sponsor Protocol Number: CACZ885M2201 | Start Date*: 2013-06-21 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled study of the safety, tolerability and effects on arterial structure and function of ACZ885 in patients with intermittent claudication | |||||||||||||
Medical condition: Peripheral Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2012-002563-10 | Sponsor Protocol Number: BAY86-4875/15961 | Start Date*: 2013-06-06 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: Multicenter open-label study to evaluate efficacy of gadobutrol-enhanced cardiac magnetic resonance imaging (CMRI) for detection of significant coronary artery disease (CAD) in subjects with known ... | ||
Medical condition: Subjects with known or suspected Coronary Artery Disease (CAD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) FR (Completed) | ||
Trial results: View results |
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: 2012-003010-14 | Sponsor Protocol Number: CACZ885M2301S1 | Start Date*: 2013-01-23 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled, event-driven trial of quarterly subcutaneous canakinumab in the prevention of recurrent cardiovascular events among stable post-myocardial infarction... | ||
Medical condition: atherosclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) GB (Prematurely Ended) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021526-36 | Sponsor Protocol Number: LMU_Rad_MR_GadoMRA01 | Start Date*: 2011-04-07 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Dynamic and high-resolution MR angiography of the supraaortic vessels at 3 Tesla: Performance of Gadobutrol (Gadovist) in comparison to Gedobenate Dimeglumine (Multihance) and Gadoterate Meglumine ... | |||||||||||||
Medical condition: Supraaortic vessel disease; suspicion or proven carotid artery stenosis / stenoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011158-17 | Sponsor Protocol Number: Hebe-2_10-02-2009 | Start Date*: 2009-08-20 |
Sponsor Name:Erasmus MC | ||
Full Title: Additional treatment to primary PCI: effects of ischemic postconditioning and Exenatide. | ||
Medical condition: Patients with a large myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005447-25 | Sponsor Protocol Number: INTIMA | Start Date*: 2013-02-22 | |||||||||||
Sponsor Name:Academic Medical Center Amsterdam, department of Internal Medicine | |||||||||||||
Full Title: The use of Rienso, an ultrasmall superparamagnetic particle of iron-oxide, as a MRI contrast agent to image inflammation in the atherosclerotic plaque | |||||||||||||
Medical condition: Atherosclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003859-12 | Sponsor Protocol Number: 12-027 | Start Date*: 2013-07-19 | ||||||||||||||||
Sponsor Name:RWTH Aachen University for the Medical Faculty, represented by Clinical Trial Center Aachen (CTC-A) | ||||||||||||||||||
Full Title: Linagliptin as a modulator of vascular inflammation in patients with type 2 diabetes mellitus | ||||||||||||||||||
Medical condition: patients with type 2 diabetes mellitus and vascular inflammation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003179-12 | Sponsor Protocol Number: MN0511_1 | Start Date*: 2012-01-09 |
Sponsor Name:University Hospital of Wuerzburg, Medical Director | ||
Full Title: Mineralocorticoid Receptor antagonists in End stage reNal DiseAse | ||
Medical condition: Hemodialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000543-27 | Sponsor Protocol Number: 19852012 | Start Date*: 2012-04-23 |
Sponsor Name:AMC | ||
Full Title: A Proof of Concept Study to Determine the Local Delivery and Efficacy of Intravenously Injected PEG-Liposomal Prednisolone Sodium Phosphate (Nanocort®) in Atherosclerotic Tissue in Subjects with Pe... | ||
Medical condition: Vessel wall inflammation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001245-32 | Sponsor Protocol Number: PGX-III-AP-002 | Start Date*: 2011-10-19 | |||||||||||
Sponsor Name:Forest Laboratories, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Trial of Apadenoson for the Detection of Myocardial Perfusion Defects Using Single-Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI) | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000171-15 | Sponsor Protocol Number: IMT-MRI-Trial-2006 | Start Date*: 2007-01-17 |
Sponsor Name:University Hospital of Ulm | ||
Full Title: Randomized, placebo-controlled, double-blinded study evaluating the effects of Pioglitazone on intima-media-thickness (IMT) of the carotid arteries measured by MRI in non-diabetic patients with con... | ||
Medical condition: Male or female non-diabetic patients at an age between 30 and 79 years (inclusive) with a proven vascular disease defined as arteriosclerosis confirmed by presence of CAD, PAD or carotid plaques. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001234-18 | Sponsor Protocol Number: NA | Start Date*: 2019-03-06 |
Sponsor Name:Imperial College NHS Trust | ||
Full Title: Effect of EVOlocumab on CARotid plaque composition in asymptomatic carotid artery stenosis (EVOCAR-1) | ||
Medical condition: Carotid stenosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
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: 2010-020497-41 | Sponsor Protocol Number: ANG.AMI-IC001 | Start Date*: 2013-02-13 | |||||||||||
Sponsor Name:Mesoblast, Inc. | |||||||||||||
Full Title: A prospective, double blind, randomized, placebo-controlled clinical trial of intracoronary infusion of immunoselected, bone marrow-derived Stro3 mesenchymal precursor cells (MPC) in the treatment ... | |||||||||||||
Medical condition: ST-elevation myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) NL (Completed) DK (Completed) SE (Completed) CZ (Completed) AT (Prematurely Ended) PL (Completed) IT (Prematurely Ended) ES (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001584-77 | Sponsor Protocol Number: MEIN/10/Ran-PCI/005 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg S.A. | |||||||||||||
Full Title: Effect of Ranolazine in ischemic patients with indication of staged interventional therapy | |||||||||||||
Medical condition: Stable Angina Pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003200-23 | Sponsor Protocol Number: 2013DR3084 | Start Date*: 2016-04-21 |
Sponsor Name:University Hospital Basel; Neurology | ||
Full Title: Biomarkers and antithrombotic treatment in cervical artery dissection (TREAT-CAD) | ||
Medical condition: cervical artery dissection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) DK (Completed) | ||
Trial results: View results |
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