- Trials with a EudraCT protocol (2,189)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
2,189 result(s) found for: Heart rate.
Displaying page 1 of 110.
EudraCT Number: 2008-007287-42 | Sponsor Protocol Number: IVA-TCMD | Start Date*: 2009-04-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PARMA | |||||||||||||
Full Title: Ivabradine in multislice CT: comparison with metoprolol in the reduction of motion artefacts and in the improvement of diagnostic care. | |||||||||||||
Medical condition: patients with coronary arteries desease, who need Tc multislice for diagnostic reasons | |||||||||||||
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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: 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: 2009-013074-41 | Sponsor Protocol Number: CRAD001ANO02 | Start Date*: 2009-11-10 | |||||||||||
Sponsor Name:Novartis Norge AS | |||||||||||||
Full Title: A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®)and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant re... | |||||||||||||
Medical condition: Heart transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003902-29 | Sponsor Protocol Number: EASI-Child | Start Date*: 2020-04-30 | |||||||||||
Sponsor Name:IRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA | |||||||||||||
Full Title: Early Administration of Ivabradine in Children with Heart Failure. | |||||||||||||
Medical condition: Acute hearth failure in dilated cardiomyopathy. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006660-30 | Sponsor Protocol Number: RO730 | Start Date*: 2009-03-11 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: Contemporary Heart Failure Management : A Randomised, Placebo-Controlled Trial to Measure the Effects of Low Dose Digoxin on Haemodynamics and Symptoms in Patients with Heart Failure | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001971-30 | Sponsor Protocol Number: CLCZ696B2317 | Start Date*: 2014-11-22 | |||||||||||
Sponsor Name:Novartis Pharma services AG | |||||||||||||
Full Title: A multicenter study to evaluate safety and tolerability in patients with chronic heart failure and reduced ejection fraction from PARADIGM-HF receiving open label LCZ696 | |||||||||||||
Medical condition: Heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) FI (Completed) NL (Completed) CZ (Completed) SE (Completed) SK (Completed) HU (Completed) PT (Completed) DK (Completed) EE (Completed) ES (Completed) IT (Completed) DE (Completed) BE (Completed) BG (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006237-27 | Sponsor Protocol Number: CT/P004/HF/08/02_01 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Torrent Pharmaceuticals Ltd. | |||||||||||||
Full Title: Safety and efficacy of TRC4186 in the treatment of stable heart failure associated with HbA1c >= 6 % or type 2 diabetes receiving oral hypoglycaemic therapy (with or without additional insulin) as ... | |||||||||||||
Medical condition: heart failure associated with impaired glucose tolerance or type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001989-15 | Sponsor Protocol Number: HomRate04_2012 | Start Date*: 2012-09-17 | |||||||||||
Sponsor Name:Universität des Saarlandes | |||||||||||||
Full Title: A randomised, placebo controlled, double blind, cross-over, single center clinical Study to investigate the effect of heart rate reduction with ivabradine on endothelial function and vascular stiff... | |||||||||||||
Medical condition: Stable coronary heart disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021844-17 | Sponsor Protocol Number: 33197 | Start Date*: 2010-12-17 | |||||||||||
Sponsor Name:Erasmus Medical Centre | |||||||||||||
Full Title: Perioperative esmolol infusion for haemodynamic stability during major vascular surgery. | |||||||||||||
Medical condition: cardiac complications during and after vascular surgery | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000269-27 | Sponsor Protocol Number: DSCK101 | Start Date*: 2014-11-06 |
Sponsor Name:German Foundation for Chronically Ill | ||
Full Title: Efficacy and tolerance of Beta Blocker and Procoralan uptitration in chronic heart failure patients under telemedical control: „70 bpm on day 28“ | ||
Medical condition: Patients with chronic heart failure and resting heart rate of ≥ 75 bmp | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004600-53 | Sponsor Protocol Number: RBK03-16-00389 | Start Date*: 2018-06-08 | ||||||||||||||||||||||||||
Sponsor Name:WÖRWAG Pharma GmbH & Co. KG | ||||||||||||||||||||||||||||
Full Title: MACH 2 - Magnesium orotate in severe congestive heart failure - Part 2 | ||||||||||||||||||||||||||||
Medical condition: Heart failure with reduced ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006337-19 | Sponsor Protocol Number: R5381-HF-2159 | Start Date*: 2022-06-08 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Doses of REGN5381, an NPR1 Agonis... | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003559-39 | Sponsor Protocol Number: 2011PP02 | Start Date*: 2013-10-01 | |||||||||||
Sponsor Name:The University of Dundee [...] | |||||||||||||
Full Title: Allopurinol and cardiovascular outcomes in patients with ischaemic heart disease (ALL-HEART) | |||||||||||||
Medical condition: Ischaemic Heart Disease (IHD), angina or myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001287-34 | Sponsor Protocol Number: BAY1067197/16718 | Start Date*: 2013-11-04 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A single blind, placebo controlled pilot study to explore the safety and tolerability of a single oral dose of 30 mg BAY 1067197 in patients with chronic heart failure on the background of preexist... | |||||||||||||
Medical condition: Heart failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001752-43 | Sponsor Protocol Number: SEVO-AIFA-FARM6H73Z9 | Start Date*: 2008-07-17 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: CARDIAC PROTECTION WITH SEVOFLURANE IN PATIENTS WITH HIGH RISK UNDERGOING HEART SURGERY. RANDOMIZED, CONTROLLED STUDY. | |||||||||||||
Medical condition: adult patients affected by cardiac valve and heart patology undergoing elective surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004186-40 | Sponsor Protocol Number: CV019-010 | Start Date*: 2020-06-18 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Randomized, Double-Blinded, Placebo-Controlled, Study to Evaluate the Safety and Tolerability of BMS-986259 in Stabilized Patients Hospitalized for Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005607-92 | Sponsor Protocol Number: QUIDHF_v3.0_20161130 | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:QUANTUM GENOMICS | |||||||||||||
Full Title: A Phase II randomized, placebo controlled, double-blind, multi-centre study to assess safety and efficacy of incremental doses of QGC001 in patients upon discharge or following hospitalization for ... | |||||||||||||
Medical condition: Patient with worsening chronic heart failure with left ventricular systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) NO (Completed) GB (Prematurely Ended) PL (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000324-17 | Sponsor Protocol Number: HULC | Start Date*: 2012-04-30 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE DI MILANO | |||||||||||||
Full Title: Administration of low doses of iodate MdC with fast speed injection in coronaric TCangiography . | |||||||||||||
Medical condition: suspected or known ischemic cardiopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001260-29 | Sponsor Protocol Number: 2012-CARDAF | Start Date*: 2012-04-24 | |||||||||||
Sponsor Name:FONDAZIONE ISTITUTO SAN RAFFAELE-G.GIGLIO | |||||||||||||
Full Title: Identification of predictive plasma Biomarkers and use of a high dosage statin during a procedure of Parrossistic Atrial Fibrillation pharmacological Cardioversion | |||||||||||||
Medical condition: Parossistic Atrial Fibrillation according to the European Socierty of Cardiology (ESC)criteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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