- Trials with a EudraCT protocol (156)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
156 result(s) found for: Angina Pectoris.
Displaying page 1 of 8.
EudraCT Number: 2010-022134-89 | Sponsor Protocol Number: CL3-06790-010 | Start Date*: 2013-11-21 | |||||||||||
Sponsor Name:I.R.I.S. | |||||||||||||
Full Title: The efficAcy and safety of Trimetazidine in Patients with angina pectoris having been treated by percutaneous Coronary Intervention. ATPCI study An international, multicentre, randomised, doub... | |||||||||||||
Medical condition: Patients with Angina pectoris having been treated by Percutaneous Coronary Intervention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) IT (Completed) LV (Prematurely Ended) ES (Completed) NL (Prematurely Ended) EE (Prematurely Ended) SK (Completed) CZ (Completed) LT (Prematurely Ended) SI (Completed) GR (Completed) DK (Prematurely Ended) PL (Completed) AT (Completed) HR (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006246-34 | Sponsor Protocol Number: CL3-16257-068 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the anti-anginal efficacy and safety of oral administration of ivabradine compared to placebo on top of a background therapy with a calcium antagonist (amlodipine or nifedipine) in pa... | |||||||||||||
Medical condition: Stable angina pectoris | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) EE (Completed) HU (Completed) PL (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004611-21 | Sponsor Protocol Number: NOM001 | Start Date*: 2008-12-29 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Does allopurinol (a xanthine oxidase inhibitor) have clinically useful anti-ischaemic effects in angina pectoris? - A randomised, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: Angina Pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001967-22 | Sponsor Protocol Number: P01799 | Start Date*: 2014-08-05 | ||||||||||||||||
Sponsor Name:Papworth Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: A phase II study to investigate the protective effects of Glucagon-like Peptide-1 (GLP-1) in patients undergoing elective angioplasty and stenting. | ||||||||||||||||||
Medical condition: To determine whether an infusion of GLP1 can reduce the occurrence of myocyte necrosis and infarction caused by percutaneous coronary intervention | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001682-17 | Sponsor Protocol Number: DRI5228 | Start Date*: 2005-01-14 | |||||||||||
Sponsor Name:Sanofi-Synthelabo-Recherche | |||||||||||||
Full Title: A Randomized Dose Ranging Study of Hexadecasaccharide including Active Control, in Patients with Unstable Angina or Non-ST-segment Elevation Myocardial Infarction Scheduled to Undergo Percutaneous ... | |||||||||||||
Medical condition: Coronary desease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009039-32 | Sponsor Protocol Number: 6368 | Start Date*: 2009-04-23 | |||||||||||||||||||||
Sponsor Name:Sahlgrenska University Hospital | |||||||||||||||||||||||
Full Title: Abciximab versus Eptifibatide versus Bivalirudin during PCI in patients with acute coronary syndromes | |||||||||||||||||||||||
Medical condition: ST elevation myocardial infarction and non ST elevation myocardial infarction/unstable angina | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005571-40 | Sponsor Protocol Number: 9207 | Start Date*: 2014-04-17 | |||||||||||||||||||||
Sponsor Name:Diagram B.V. | |||||||||||||||||||||||
Full Title: Randomized Evaluation of short-term DUal anti platelet therapy in patients with acute coronary syndrome treated with the COMBO dual-therapy stEnt | |||||||||||||||||||||||
Medical condition: Acute coronary syndrome | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) DE (Completed) HU (Completed) IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001960-30 | Sponsor Protocol Number: CL3-16257-057 | Start Date*: 2005-03-07 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the anti-anginal efficacy and safety of oral administration of ivabradine compared to placebo on top of a background therapy with atenolol in patients with stable angina pectoris. A 4... | |||||||||||||
Medical condition: stable angina pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) NO (Completed) SE (Completed) SK (Completed) CZ (Completed) GB (Completed) IT (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002208-17 | Sponsor Protocol Number: DNB-001-CT002 | Start Date*: 2007-08-14 | ||||||||||||||||
Sponsor Name:Danube Pharmaceuticals | ||||||||||||||||||
Full Title: A Phase IIa, Multi-Center, Double Blind, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy, Safety and Pharmacokinetics of DNB-001 in Patients with Angina Pectoris and Moderate Chronic ... | ||||||||||||||||||
Medical condition: Angina pectoris and renal insufficiency whilst undergoing percutaneous coronary intervention (PCI). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003149-24 | Sponsor Protocol Number: Ranolazine¿AOUPi/001 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: Ranolazine in patients with post systolic thickening due to stable effort angina: a phase II, randomized, open-label, standard therapy controlled, parallel group study assessing the effects on left... | |||||||||||||
Medical condition: Stable angina with normal ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002456-18 | Sponsor Protocol Number: 758-CL-010 | Start Date*: 2006-04-21 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE SAFETY, TOLERABILITY AND PRELIMINARY EFFICACY OF A FOUR-WEEK TREATMENT WITH YM758 IN SUBJECTS WITH STABLE ANGINA. | |||||||||||||
Medical condition: Stable angina pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000197-19 | Sponsor Protocol Number: NCT02032303 | Start Date*: 2015-07-23 | |||||||||||||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||||||||||||
Full Title: Assessment of Coronary Flow Reserve by Doppler Flow WIre in Patients With Acute Coronary Syndrome Undergoing PercuTaneous Coronary Intervention: DiffErences Between the LoAding Dose of Ticagrelor a... | |||||||||||||||||||||||
Medical condition: Patients with acute coronary syndrome | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002803-37 | Sponsor Protocol Number: XC001-1001 | Start Date*: 2022-01-20 | |||||||||||
Sponsor Name:XyloCor Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 1/2 Trial of Direct Administration of AdVEGF-All6A+, a Replication Deficient Adenovirus Vector Expressing a cDNA/Genomic Hybrid of Human Vascular Endothelial Growth Factor, to the Ischemic ... | |||||||||||||
Medical condition: Angina Pectoris Secondary | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015826-13 | Sponsor Protocol Number: Q-10 | Start Date*: 2010-10-07 | |||||||||||
Sponsor Name:PROF. TIZIANO GHERLI | |||||||||||||
Full Title: THE USE OF COENZYME Q 10 BEFORE HEART SURGERY IN ELDERLY PATIENTS. | |||||||||||||
Medical condition: Patients (male or female) aged > 70 years, clinically stable, with a diagnosis of severe aortic stenosis with indication to surgery based on echocardiography and left ventricle angiography. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005435-98 | Sponsor Protocol Number: version_2.0_dated_19.04.2011 | Start Date*: 2012-06-21 | |||||||||||
Sponsor Name:Śląski Uniwersytet Medyczny w Katowicach | |||||||||||||
Full Title: A randomized, prospective, double-blind study with placebo to evaluate the efficacy of treatment of patients with angina resistant to pharmacological treatment and induced myocardial ischemia with... | |||||||||||||
Medical condition: Stable angina pectoris CCS II-IV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005475-17 | Sponsor Protocol Number: CL3-16257-067 | Start Date*: 2008-01-04 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S.) | |||||||||||||
Full Title: Long-term (3 years) ophthalmic safety and cardiac efficacy and safety of ivabradine administered orally at the therapeutic doses (2.5/5/7.5 mg b.i.d.) on top of anti-anginal background therapy, to ... | |||||||||||||
Medical condition: Stable angina pectoris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) PT (Completed) BE (Completed) FI (Completed) GB (Prematurely Ended) HU (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000789-31 | Sponsor Protocol Number: RGH201 | Start Date*: 2018-02-09 | |||||||||||
Sponsor Name:Kuopio University Hospital Heart Center | |||||||||||||
Full Title: Clinical development and proof of principle testing of new regenerative VEGF-D therapy for cost-effective treatment of refractory angina. A phase II randomized, double-blinded, placebo-controlled s... | |||||||||||||
Medical condition: Refractory angina | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003260-37 | Sponsor Protocol Number: 1060 | Start Date*: 2015-10-22 | ||||||||||||||||||||||||||
Sponsor Name:Liverpool Heart and Chest Hospital | ||||||||||||||||||||||||||||
Full Title: Can Ivabradine attenuate post-revascularisation microcirculatory dysfunction in flow limiting coronary artery disease? | ||||||||||||||||||||||||||||
Medical condition: Coronary Artery Disease/Angina | ||||||||||||||||||||||||||||
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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: 2015-002153-35 | Sponsor Protocol Number: GAP | Start Date*: 2015-09-10 | |||||||||||
Sponsor Name:Bispebjerg University Hospital | |||||||||||||
Full Title: Effect of Glucagon-like peptide-1 stimulation on coronary microvascular dysfunction in women with angina pectoris and no obstructive stenosis of major coronary vessels | |||||||||||||
Medical condition: Patients with angina pectoris and coronary microvascular dysfunction without significant stenosis og major coronary vessels | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017924-18 | Sponsor Protocol Number: P10 | Start Date*: 2011-01-04 |
Sponsor Name: | ||
Full Title: Efficacy assessment of repeat intramyocardial injection of autologous bone marrow cells in previously responding no-option patients with residual refractory angina pectoris and documented ischemia | ||
Medical condition: In coronary artery disease atherosclerosis leads to a decrease in lumen diameter of the large epicardial arteries, causing a deficit in blood flow known as ischemia. This ischemia can cause chest p... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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