- Trials with a EudraCT protocol (901)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
901 result(s) found for: Cardiovascular Diseases AND Heart Disease.
Displaying page 1 of 46.
EudraCT Number: 2009-017242-30 | Sponsor Protocol Number: D5132C00001 | Start Date*: 2010-12-06 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled, Parallel Group, Multinational Trial, to Assess the Prevention of Thrombotic Events with Ticagrelor Compared to Placebo on a Background of Acetyl Sali... | |||||||||||||
Medical condition: Myocardial Infarction, Cardiovascular Death, Atherothombosis, Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) DE (Completed) HU (Completed) RO (Completed) CZ (Completed) SK (Completed) PL (Completed) BE (Completed) ES (Completed) SE (Completed) IT (Completed) NO (Completed) BG (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: 2017-002644-32 | Sponsor Protocol Number: EFC14875 | Start Date*: 2017-11-14 | ||||||||||||||||
Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Demonstrate the Effects of Sotagliflozin on Cardiovascular and Renal Events in Patients with Type 2 Diabetes, Ca... | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus Chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Prematurely Ended) LV (Completed) GB (Completed) HU (Completed) SE (Completed) NO (Completed) FR (Completed) NL (Completed) DK (Completed) ES (Prematurely Ended) LT (Completed) EE (Completed) PT (Completed) BE (Completed) GR (Completed) BG (Completed) IT (Completed) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000880-18 | Sponsor Protocol Number: ESR-15-11524 | Start Date*: 2016-08-01 | ||||||||||||||||
Sponsor Name:Special Account for Research Funds-University of Patras | ||||||||||||||||||
Full Title: A randomized, pharmacodynamic comparison of low dose ticagrelor to clopidogrel in patients with prior myocardial infarction | ||||||||||||||||||
Medical condition: The primary objective of the study is to compare the platelet inhibition of ticagrelor versus clopidogrel in post-MI patients in terms of platelet reactivity at the end of the 2 study periods (pre... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 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: 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: 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: 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: 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: 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: 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: 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: 2017-005066-22 | Sponsor Protocol Number: CTSU_MDCO-PCS-17-01 | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:University of Oxford [...] | |||||||||||||
Full Title: HPS-4/TIMI 65/ORION-4: A double-blind randomized placebo-controlled trial assessing the effects of inclisiran on clinical outcomes among people with atherosclerotic cardiovascular disease | |||||||||||||
Medical condition: Atherosclerotic cardiovascular disease | |||||||||||||
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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: 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: 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: 2013-000046-19 | Sponsor Protocol Number: RIVAROXHFA3001/BAY59-7939/16302 | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Event-driven, Multicenter Study Comparing the Efficacy and Safety of Oral Rivaroxaban with Placebo for Reducing the Risk of Death, Myocardial Infarction or Stroke in Sub... | |||||||||||||
Medical condition: Prevention of death, heart attack and stroke in patients with chronic heart failure and significant coronary artery disease following a hospitalization for exacerbation of heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) NL (Completed) BG (Completed) PL (Completed) HU (Completed) SE (Completed) IT (Completed) GB (Completed) EE (Completed) LT (Completed) PT (Completed) DK (Completed) LV (Completed) SK (Completed) GR (Completed) | |||||||||||||
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: 2012-005359-18 | Sponsor Protocol Number: RIVENDEL | Start Date*: 2013-01-22 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Heart Rate reduction by IVabradine for improvement of ENDothELial function in patients with coronary artery disease: the RIVENDEL study | |||||||||||||
Medical condition: PATIENTS WITH CAD AFTER CORONARY ANGIOPLASTY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000887-27 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-05-23 | |||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||||||||||||
Full Title: Pilot Trial: The effects of intravenous heme arginate on HO-1 expression and oxidative stress in the human heart | |||||||||||||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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