- Trials with a EudraCT protocol (514)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
514 result(s) found for: cardiac MRI.
Displaying page 1 of 26.
| EudraCT Number: 2015-005384-16 | Sponsor Protocol Number: FLORAMICAR | Start Date*: 2016-04-26 | ||||||||||||||||
| Sponsor Name:FONDAZIONE TOSCANA GABRIELE MONASTERIO | ||||||||||||||||||
| Full Title: A prospective single-arm, monocentric, phase-II explorative study on evaluation of diagnostic use of the PET tracer (18F)-florbetaben (Neuraceq®) in patient with patient with suspected cardiac amyl... | ||||||||||||||||||
| Medical condition: Patients with high clinical suspicion of cardiac amyloidosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-001134-33 | Sponsor Protocol Number: iCHF | Start Date*: 2012-11-21 | |||||||||||
| Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
| Full Title: Randomized, Double-Blind, Placebo-Controlled Trial of Ferric Carboxymaltose Versus Placebo in Patients with Congestive Heart Failure | |||||||||||||
| Medical condition: Congestive heart failure (CHF) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001109-28 | Sponsor Protocol Number: pgrf/141/09 | Start Date*: 2008-05-23 | |||||||||||||||||||||
| Sponsor Name:University of Aberdeen | |||||||||||||||||||||||
| Full Title: Perhexiline therapy in patients with heart failure with preserved left ventricular ejection fraction(HFpEF syndrome) | |||||||||||||||||||||||
| Medical condition: Heart failure with preserved left ventricular ejection fraction | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2009-013103-63 | Sponsor Protocol Number: 1884 | Start Date*: 2011-12-14 | |||||||||||
| Sponsor Name:Asklepios Kliniken Hamburg GmbH | |||||||||||||
| Full Title: Pilot study investigating the effect of intra-coronary and intra-myocardial application of enriched CD133pos autologous bone marrow derived stem cells for improving left ventricular function in chr... | |||||||||||||
| Medical condition: Patients with chronic ischemic cardiomyopathy with an LVEF ≤45% and symptomatic heart failure NYHA ≥ II under optimal therapy and drug treatment according to the current ESC heart failure guidelines. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004277-41 | Sponsor Protocol Number: 16.0012 | Start Date*: 2017-01-18 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:St George's University of London | ||||||||||||||||||||||||||||||||||||||
| Full Title: An observational study into the variety of electrocardiographic responses to an ajmaline Provocation in healthy subjects. What are the genetic and structural variations dictating this response ? | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Study in the healthy population. This is a study of a test used in the diagnosis of the condition, Brugada Syndrome. | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-003461-41 | Sponsor Protocol Number: HP4.3 | Start Date*: 2007-11-13 |
| Sponsor Name:Deutsche Herzzentrum Berlin, Kompetenznetz Angeborene Herzfehler | ||
| Full Title: Cardiac imaging under dobutamine stress for early assessment of right ventricular function in patients with tetralogy of Fallot and pulmonary regurgitation | ||
| Medical condition: Fallot tetralogy late after repair with marked pulmonary valve incompetence | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004492-40 | Sponsor Protocol Number: COHERENT | Start Date*: 2021-02-03 | ||||||||||||||||
| Sponsor Name:Cardiovascular Non-Invasive Imaging Research Laboratory, Department of Cardiology, Herlev and Gentofte Hospital | ||||||||||||||||||
| Full Title: COHERENT - The COlchicine HypERtENsion Trial | ||||||||||||||||||
| Medical condition: Hypertension | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-005109-19 | Sponsor Protocol Number: ATTICUS | Start Date*: 2015-11-10 |
| Sponsor Name:University Hospital Tuebingen | ||
| Full Title: Apixaban for treatment of embolic stroke of undetermined source | ||
| Medical condition: Patients with embolic stroke of undetermined source and at least on risk factor for cardiac embolism | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000246-62 | Sponsor Protocol Number: CICL670AAU01 | Start Date*: 2016-03-07 | |||||||||||
| Sponsor Name:Novartis | |||||||||||||
| Full Title: A Study of Magnetic Resonance Imaging Assessment of Cardiac and Liver Iron Load in Patients With Haemoglobinopathies, Myelodysplastic Syndromes (MDS) or Other Anaemias Treated With Exjade® (Deferas... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004054-24 | Sponsor Protocol Number: PHRCN2017/CAPRI-MARIE/NK | Start Date*: 2019-03-18 | |||||||||||
| Sponsor Name:Centre Hospitalier Régional Universitaire de Nancy | |||||||||||||
| Full Title: Assessment of the (18)F-florbetaben whole-body PET imaging diagnostic performance for the detection of cardiac and extracardiac sites of amyloid deposits in patients with amyloidosis | |||||||||||||
| Medical condition: cardiac amyloidosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000867-10 | Sponsor Protocol Number: CD13/10671 | Start Date*: 2014-02-13 | |||||||||||||||||||||
| Sponsor Name:University of Leeds | |||||||||||||||||||||||
| Full Title: Effects of Aldosterone Antagonism in Heart Failure with Preserved Ejection Fraction (HF-PEF): Cardiac MRI, Echocardiography, Exercise Physiology & Quality of Life Assessment | |||||||||||||||||||||||
| Medical condition: Heart failure with a preserved ejection fraction | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-002628-29 | Sponsor Protocol Number: R&D6327 | Start Date*: 2014-09-09 |
| Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
| Full Title: Evaluating the effectiveness of intravenous ciclosporin on reducing reperfusion injury in patients undergoing primary percutaneous coronary intervention: a double-blind, phase II, randomised contro... | ||
| Medical condition: Myocardial ischemia/reperfusion injury | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004805-29 | Sponsor Protocol Number: 201200480529 | Start Date*: 2013-06-04 | |||||||||||
| Sponsor Name:The Heart Center, Rigshospitalet | |||||||||||||
| Full Title: Beta 3 agonist treatment in heart failure (BEAT-HF) | |||||||||||||
| Medical condition: Systolic heart failure | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003230-22 | Sponsor Protocol Number: CICL670AIT07 | Start Date*: 2008-11-04 | |||||||||||
| Sponsor Name:NOVARTIS FARMA | |||||||||||||
| Full Title: Multicenter, open label, prospective study to evaluate the efficacy and safety of deferasirox 30 mg/kg/day for 52 weeks, in transfusion-dependent β-thalassemic patients with cardiac MRI ... | |||||||||||||
| Medical condition: cardiac iron overload | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004706-33 | Sponsor Protocol Number: RH-HJE-LN-01 | Start Date*: 2017-03-31 | |||||||||||
| Sponsor Name:Finn Gustafsson | |||||||||||||
| Full Title: The Effect of Ivabradine Treatment on Exercise Capacity in Patients with Cardiac Allograft Vasculopathy after Heart Transplantation | |||||||||||||
| Medical condition: Cardiac allograft vasculopathy and elevated resting heart rate in heart transplant recipients | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000885-39 | Sponsor Protocol Number: 02289 | Start Date*: 2021-01-12 | |||||||||||
| Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
| Full Title: Safety and Efficacy of Induced Pluripotent Stem Cell-derived Engineered Human Myocardium as Biological Ventricular Assist Tissue in Terminal Heart Failure | |||||||||||||
| Medical condition: Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001850-42 | Sponsor Protocol Number: MSC3 | Start Date*: 2008-06-16 | |||||||||||
| Sponsor Name:The Heart Centre, Rigshospitalet | |||||||||||||
| Full Title: Autolog mesenkymal stromal cellebehandling af patienter med hjertesvigt. | |||||||||||||
| Medical condition: Congestive heart failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003146-75 | Sponsor Protocol Number: BETA3_LVH | Start Date*: 2016-03-14 | |||||||||||
| Sponsor Name:Université catholique de Louvain (UCL) | |||||||||||||
| Full Title: A multi-centre randomized, placebo-controlled trial of mirabegron, a new beta3-adrenergic receptor agonist on the progression of left ventricular mass and diastolic function in patients with struct... | |||||||||||||
| Medical condition: Structural heart disease at high risk for progressive hypertrophic cardiac remodeling at risk of developing HFpEF (heart failure with preserved ejection fraction). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) GR (Completed) PL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002813-33 | Sponsor Protocol Number: ARMYDA-9DAPAtrial | Start Date*: 2023-02-21 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA MAGGIORE DELLA CARITà DI NOVARA | ||||||||||||||||||
| Full Title: Early use of dapaglifozin in diabetic patients with acute myocardial infarction and reduced ejection fraction: the randomized ARMYDA-9 DAPA trial | ||||||||||||||||||
| Medical condition: Patients with type 2 diabetes and ST-elevation myocardial infarction treated with primary primary percutaneous coronary intervention and reduced left ventricle ejection fraction. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-003372-31 | Sponsor Protocol Number: LJ401-BT01 | Start Date*: 2018-03-20 | |||||||||||
| Sponsor Name:La Jolla Pharmaceutical Company | |||||||||||||
| Full Title: A Multi-center, Randomized, Open-Label, Parallel-Group Study with LJPC-401 for the Treatment of Myocardial Iron Overload in Patients with Transfusion-Dependent Beta Thalassemia | |||||||||||||
| Medical condition: Transfusion-dependent beta thalassemia with myocardial iron overload | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) GR (Completed) CY (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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