- Trials with a EudraCT protocol (30)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
30 result(s) found for: Intravascular imaging.
Displaying page 1 of 2.
EudraCT Number: 2005-004325-25 | Sponsor Protocol Number: MS325-19 | Start Date*: 2007-01-04 |
Sponsor Name:Administration management, Ludwig-Maximilians-University of Munich | ||
Full Title: Comprehensive whole-body 3T MRA of Patients with Low or Moderate Clinical Probability for Pulmonary Embolism using an Intravascular MR Contrast Agent Vasovist® | ||
Medical condition: Patients with low or moderate clinical probability for pulmonary embolism and positive or negative CTA for pulmonary embolism after CT and sonographic examination for deep venous thrombosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002304-16 | Sponsor Protocol Number: 130873-2004 | Start Date*: 2005-06-14 |
Sponsor Name:South Tees Hospitals NHS Foundation Trust | ||
Full Title: The STARS (STeroids Against Re-Stenosis) Trial [THE USE OF Peri-PROCEDURAL ORAL CORTICOSTERIODS TO PREVENT IN-SEGMENT RESTENOSIS AFTER PERCUTANEOUS CORONARY INTERVENTION.] | ||
Medical condition: coronary artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (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: 2004-000712-42 | Sponsor Protocol Number: IOM-115 | Start Date*: 2004-12-22 |
Sponsor Name:Bracco Imaging S.p.A. | ||
Full Title: Enhacement of the lower extremities computed tomography: IOMERON®-400 VS VISIPAQUE™-320 (ELECTIV). | ||
Medical condition: subjects with mild to moderate renal impairment (SCr =1.5-2.5 mg/dL and/or calculated CrCl = 10-60 mL/min) who undergo clinically-indicated IV contrast-enhanced MDCTA scanning of the lower extremit... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Completed) GB (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-003234-32 | Sponsor Protocol Number: UKM13_0018 | Start Date*: 2014-12-02 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: Pathological changes in the myocardial microvasculature - a MR-based quantification | ||
Medical condition: Patients with cardiovascular diseases and suspect of myocardial microvasculopathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001905-66 | Sponsor Protocol Number: BA-SCAD | Start Date*: 2021-07-06 |
Sponsor Name:Spanish Cardiology Society | ||
Full Title: Randomized clinical trial assessing the value of Beta-Blockers and Antiplatelet Agents in patients with Spontaneous Coronary Artery Dissection | ||
Medical condition: Spontaneous Coronary Artery Dissection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000013-36 | Sponsor Protocol Number: 49653/416 | Start Date*: 2005-08-17 |
Sponsor Name:Dr. Olivier F. Bertrand , Laval Hospital | ||
Full Title: A Multicenter Randomized Double-Blind Trial Comparing Rosiglitazone to Placebo for the Prevention of Atherosclerosis Progression after Coronary Bypass Surgery in Diabetic Patients | ||
Medical condition: Atherosclerosis progression in vein grafts in diabetic patients after coronary bypass surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001502-15 | Sponsor Protocol Number: 2016-01382 | Start Date*: 2017-12-13 | |||||||||||
Sponsor Name:Insel Gruppe AG - Inselspital | |||||||||||||
Full Title: Effects of the PCSK9 Antibody AliroCuMab on Coronary Atherosclerosis in PatieNts with Acute Myocardial Infarction. A Serial, Multivessel, Intravascular Ultrasound, Near-Infrared Spectroscopy And Op... | |||||||||||||
Medical condition: Patients presenting with acute myocardial infarction (non-ST-elevation myocardial infarction or acute ST-elevation myocardial infarction) and with elevated cholesterol levels. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2025-000122-33 | Sponsor Protocol Number: 5354-CL-0301 | Start Date*: 2025-04-16 | |||||||||||
Sponsor Name:Astellas Pharma Global Development Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Prospective, Randomized, Open label Study for Intraoperative Ureter(s) Visualization When Using ASP5354 with Near infrared Fluorescence (NIR-F) Imaging in Participants Under... | |||||||||||||
Medical condition: visualisation of ureter | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000826-13 | Sponsor Protocol Number: MDCO-APO-15-01 | Start Date*: 2016-01-20 |
Sponsor Name:The Medicines Company | ||
Full Title: A placebo-controlled, double-blind, randomized trial to compare the effect of treatment on plaque burden as determined by intravascular ultrasound and to evaluate the efficacy, pharmacokinetics, sa... | ||
Medical condition: acute coronary syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) HU (Completed) NL (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004727-18 | Sponsor Protocol Number: CORUNO/II/05.1 | Start Date*: 2008-06-20 | |||||||||||
Sponsor Name:THERABEL PHARMACEUTICAL Ltd | |||||||||||||
Full Title: EFFECT OF MOLSIDOMINE 16 MG ADMINISTERED ONCE-DAILY AS A LONG-TERM ADD-ON TREATMENT, ON ATHEROSCLEROSIS PROGRESSION AND INFLAMMATORY BIOMARKERS IN PATIENTS HOSPITALIZED FOR ACUTE CORONARY SYNDROME. | |||||||||||||
Medical condition: Randomized, double-blind, placebo-controlled, add-on study in two parallel groups. Patients admitted for Non ST Segment Elevation Acute Coronary Syndromes will undergo a coronary angiography accord... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
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: 2014-005462-30 | Sponsor Protocol Number: MDCO-APO-14-01 | Start Date*: 2016-10-26 |
Sponsor Name:The Medicines Company | ||
Full Title: A multiple dose, dose-finding, placebo controlled, double blind, randomized trial to compare the effect of treatment on plaque burden as determined by intravascular ultrasound and evaluate the effi... | ||
Medical condition: acute coronary syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001656-35 | Sponsor Protocol Number: LIFE-02-MF | Start Date*: 2019-01-10 | |||||||||||
Sponsor Name:Dept.Dermotology , Aarhus University | |||||||||||||
Full Title: Metabolic imaging of patients with mycosis fungoides using hyperpolarized 13C-Pyruvate magnetic resonance imaging – A feasibility study | |||||||||||||
Medical condition: mycosis fungiodes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004372-27 | Sponsor Protocol Number: 0112 | Start Date*: 2016-05-17 | |||||||||||
Sponsor Name:Theravance Biopharma Ireland Limited | |||||||||||||
Full Title: A Phase 3 Multicenter, Randomized, Open-label, Clinical Trial of Telavancin Versus Standard Intravenous Therapy in the Treatment of Subjects with Staphylococcus aureus Bacteremia Including Infectiv... | |||||||||||||
Medical condition: Staphylococcus aureus Bacteremia Including Infective Endocarditis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) PL (Completed) LV (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2019-003087-43 | Sponsor Protocol Number: SAFER | Start Date*: 2021-01-12 | |||||||||||
Sponsor Name:Synektik Spółka Akcyjna | |||||||||||||
Full Title: A Phase I/II Seamless Adaptive, Open label study to assess Safety, Tolerability, Radiation Dosimetry, Biodistribution, and diagnostic ability of a Novel 18F-labelled Tracer, SYN2, for Positron Emis... | |||||||||||||
Medical condition: phase II: suspected coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002076-41 | Sponsor Protocol Number: 0667 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:University of Leicester | ||||||||||||||||||
Full Title: A RANDOMISED CONTROLLED TRIAL OF PRE-SURGERY SODIUM VALPROATE, FOR THE PREVENTION OF ORGAN INJURY IN CARDIAC SURGERY: Val-CARD | ||||||||||||||||||
Medical condition: Reduction of myocardial and kidney injury risk of post cardiac surgery by increasing the expression of genes that promote myocardial mitochondrial homeostasis via effects on chromatin histone deace... | ||||||||||||||||||
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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: 2018-000775-32 | Sponsor Protocol Number: AB.OH.2018 | Start Date*: 2018-06-05 | |||||||||||
Sponsor Name:Vall d'Hebron Institut de Recerca | |||||||||||||
Full Title: Phase IV, randomized, open, parallel groups clinical trial for evaluating the early Stop of antibiotic Treatment in febrile neutropenic Oncohematological Paediatric patients. | |||||||||||||
Medical condition: Febrile neutrophenia in oncohematological pediatric patients. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001582-33 | Sponsor Protocol Number: Er-01-Perf-Stroke | Start Date*: 2012-09-19 |
Sponsor Name:University Hospital Erlangen | ||
Full Title: Intraindividual cross-over comparison of Gadobutrol and Gadoterate enhanced combined DSC-MR-Perfusion and MR-Angiography in patients with cerebrovascular disease | ||
Medical condition: Patients with high grade carotid artery stenosis or acute cerebral ischemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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