- Trials with a EudraCT protocol (2,084)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (429)
2,084 result(s) found for: Cardiovascular Disease.
Displaying page 1 of 105.
EudraCT Number: 2018-001917-34 | Sponsor Protocol Number: TropO2 | Start Date*: 2018-12-14 | ||||||||||||||||
Sponsor Name:Consorci Mar Parc de Salut de Barcelona | ||||||||||||||||||
Full Title: Cardiac complications associated to perioperative hyperoxia in elective colorectal surgery | ||||||||||||||||||
Medical condition: Cardiovascular complications after colorectal surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012269-71 | Sponsor Protocol Number: BC22140 | Start Date*: 2010-03-08 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: Cardiovascular outcomes study to evaluate the potential of aleglitazar to reduce cardiovascular risk in patients with a recent acute coronary syndrome (ACS) event and type 2 diabetes mellitus (T2D) | |||||||||||||
Medical condition: Type 2 diabetes patients with a recent acute coronary syndrome (ACS) event | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Temporarily Halted) SE (Prematurely Ended) DK (Prematurely Ended) FR (Completed) IE (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001891-21 | Sponsor Protocol Number: NC25608 | Start Date*: 2012-02-21 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Phase 3b, Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group, Study to Evaluate the Effect of Dalcetrapib 600 mg on Cardiovascular (CV) Events in Adult Patients with Stable Coronary H... | |||||||||||||
Medical condition: Patients with stable CHD, CHD risk equivalents (including PAD, cerebrovascular disease, and T2D), or at elevated risk for CV mortality and morbidity on the basis of multiple risk factors for CVD by... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) PL (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007638-21 | Sponsor Protocol Number: CR2 | Start Date*: 2008-09-04 | ||||||||||||||||
Sponsor Name:University of Aberdeen [...] | ||||||||||||||||||
Full Title: Is cessation of clopidogrel therapy associated with rebound of platelet activity in stable vascular disease patients? | ||||||||||||||||||
Medical condition: Cardiovascular disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006875-35 | Sponsor Protocol Number: HMARAAS1 | Start Date*: 2009-10-27 | |||||||||||
Sponsor Name:IMAS | |||||||||||||
Full Title: Administración perioperatoria de aspirina a baja dosis como prevención secundaria de muerte súbita, apoplejía, infarto de miocardio y otros accidentes isquémicos postoperatorios. Ensayo clínico mul... | |||||||||||||
Medical condition: Paciente con indicación quirúrgica electiva de riesgo cardiovascular intermedio (cirugía oncológica con apertura del abdomen y/o tórax como, artroplastia de cadera o rodilla) y que esté recibiendo ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002257-19 | Sponsor Protocol Number: CARDIORYC-2014-001 | Start Date*: 2015-04-21 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Ramón y Cajal | |||||||||||||
Full Title: Single-center, randomized, open, controlled by echocardiography to evaluate the effect of serelaxina in the functioning of the right ventricle and its potential in the prognosis of acute heart fail... | |||||||||||||
Medical condition: ICA hospitalized patients with high normal blood pressure, and mild to moderate renal failure at the time of selection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022641-25 | Sponsor Protocol Number: MASTER2010 | Start Date*: 2011-07-11 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||||||||||||
Full Title: Maraviroc Abacavir STudy – effect on Endothelial Recovery | ||||||||||||||||||||||||||||
Medical condition: -Human Imunodeficiency Virus (HIV) infection -Endothelial dysfunction in HIV-infected patients -immune activation in HIV-infected patients -cardiovascular complications in HIV-infecetd patients | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001076-11 | Sponsor Protocol Number: CTQJ230A12301 | Start Date*: 2019-12-19 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized double-blind, placebo-controlled, multicenter trial assessing the impact of lipoprotein (a) lowering with pelacarsen (TQJ230) on major cardiovascular events in patients with establishe... | |||||||||||||
Medical condition: Cardiovascular Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) SK (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) PT (Trial now transitioned) SE (Trial now transitioned) NL (Ongoing) BG (Trial now transitioned) BE (Trial now transitioned) NO (Trial now transitioned) SI (Trial now transitioned) RO (Trial now transitioned) IS (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005532-32 | Sponsor Protocol Number: KWI-NIC-02 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Kwizda Pharma | |||||||||||||
Full Title: The bioavailability of nicorandil in humans: A pilot study to investigate the variability of its pharmacokinetic parameters in healthy volunteers. | |||||||||||||
Medical condition: The bioavailability of Nicorandil in humans: A pilot study to investigate the variability of the pharmacokinetic parameters in healthy volunteers. The IMP Nicorandil (2-(pyridine-3-carbonylamino)et... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012270-12 | Sponsor Protocol Number: BC22419 | Start Date*: 2010-05-21 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: Effects of 150 μg aleglitazar on renal function in patients with Type 2 diabetes and moderate renal impairment, as compared to Actos® | |||||||||||||
Medical condition: Type 2 diabetes with moderate renal function impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000215-89 | Sponsor Protocol Number: CL2-16257-099 | Start Date*: 2013-06-14 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Effects of ivabradine on vascular function in individuals at increased risk of developing cardiovascular disease and with impaired endothelial function An international, multicentre, randomised, d... | |||||||||||||
Medical condition: Cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001743-31 | Sponsor Protocol Number: NL43882.029.13 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: The cardiovascular effects of hyperoxia during and shortly after CABG surgery | |||||||||||||
Medical condition: During and after coronary artery bypass graft operation we will investigate the cardiovascular effects of hyperoxia on blood pressure, cardiac function, microcirculation and ischemia/reperfusion. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003946-34 | Sponsor Protocol Number: OB-401 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:VIVUS, Inc. | |||||||||||||
Full Title: A Qsymia™ CardiovascuLAr morbIdity and Mortality (AQCLAIM) Study in Subjects with Documented Cardiovascular Disease | |||||||||||||
Medical condition: Cardiovascular Disease in overweight and obese subjects | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006922-32 | Sponsor Protocol Number: HOADO | Start Date*: 2009-02-09 | |||||||||||
Sponsor Name:RUNMC | |||||||||||||
Full Title: Heme oxygenase (HO) activity in humans. Effects of heme arginate (Normosang®) on parameters of HO activity and on adenosine induced vasodilation. | |||||||||||||
Medical condition: Normosang treatment will be used to evaluate heme oxygenase induction in healthy subjects. Results will be used for future studies concerning diabetes related cardiovascular disease. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001069-18 | Sponsor Protocol Number: 12/0533 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:University College London (UCL) | |||||||||||||
Full Title: MINeralocorticoid receptor antagonist pretreatment to MINIMISE reperfusion injury after ST-Elevation Myocardial Infarction(STEMI). | |||||||||||||
Medical condition: Cardiovascular disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002466-35 | Sponsor Protocol Number: ACTRN012607000099426 | Start Date*: 2008-03-11 | |||||||||||
Sponsor Name:Imperial Ciollege [...] | |||||||||||||
Full Title: A randomised placebo-controlled trial of fixed-dose combination medication in those at raised risk of cardiovascular disease | |||||||||||||
Medical condition: Cardiovascular Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003000-39 | Sponsor Protocol Number: CL2-38844-010 | Start Date*: 2014-03-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the pharmacodynamics, pharmacokinetics and safety of repeated escalating oral doses of S 38844 versus placebo in patients with chronic heart failure and left ventricular systolic d... | |||||||||||||
Medical condition: Patients with chronic heart failure and left ventricular systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) SK (Completed) EE (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001682-12 | Sponsor Protocol Number: MYOFLAME-19 | Start Date*: 2023-06-16 | ||||||||||||||||
Sponsor Name:Goethe University Frankfurt | ||||||||||||||||||
Full Title: Randomised placebo controlled clinical trial of efficacy of MYOcardial protection with postacute inFLAMmatory cardiac involvEment due to COVID-19 (MYOFLAME-19) | ||||||||||||||||||
Medical condition: Inflammatory cardiovascular involvement due to COVID-19, defined by Cardiovascular magnetic resonance imaging | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005288-33 | Sponsor Protocol Number: EMI111784 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development, LtdD | |||||||||||||
Full Title: Methodology Study to develop Sinerem enhanced 3T MR Imaging of Atherosclerotic Plaques within the Carotid Arteries, and to compare Sinerem MRI to contrast enhanced ultrasound | |||||||||||||
Medical condition: Atherosclerotic plaque within the carotid artery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003486-26 | Sponsor Protocol Number: 1002-047 | Start Date*: 2017-05-24 | ||||||||||||||||
Sponsor Name:Esperion Therapeutics Inc., | ||||||||||||||||||
Full Title: A Long-term, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy of Bempedoic Acid (ETC-1002) in Patients with Hyperlipidemia at High Cardiovascular Risk Not Ad... | ||||||||||||||||||
Medical condition: Patients with Hyperlipidemia at High Cardiovascular Risk Not Adequately Controlled by Their Lipid-Modifying Therapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
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