- Trials with a EudraCT protocol (237)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
237 result(s) found for: Percutaneous coronary intervention.
Displaying page 2 of 12.
EudraCT Number: 2021-001418-12 | Sponsor Protocol Number: NCT04483583 | Start Date*: 2021-06-24 |
Sponsor Name:University of Florida | ||
Full Title: Tailoring P2Y12 Inhibiting Therapy in Patients requiring Oral Anticoagulation after undergoing Percutaneous Coronary Intervention: The Switching Anti-Platelet and Anti-Coagulant Therapy – 2 Study | ||
Medical condition: Efficacy of antiplatelet therapy after percutaneous coronary intervention in patients using oral anticoagulants | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014176-22 | Sponsor Protocol Number: H7T-MC-TADF | Start Date*: 2010-03-10 | |||||||||||
Sponsor Name:Eli Lilly | |||||||||||||
Full Title: A Comparison of Prasugrel at the Time of Percutaneous Coronary Intervention (PCI) Or as Pre-treatment At the Time of Diagnosis in Patients with Non-ST-Elevation Myocardial Infarction (NSTEMI) - T... | |||||||||||||
Medical condition: Acute Coronary Syndromes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) FR (Completed) FI (Completed) HU (Completed) SE (Completed) SK (Completed) IT (Completed) DE (Prematurely Ended) PL (Completed) CZ (Completed) DK (Prematurely Ended) PT (Completed) AT (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019688-12 | Sponsor Protocol Number: abchits2010 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:Friedrich-Schiller University Jena, Clinic for Internal Medicine I | |||||||||||||
Full Title: Prospective placebo controlled trial: Detection of coronary microembolization by Doppler ultrasound in patients with stable angina pectoris during percutaneous coronary interventions under an adjun... | |||||||||||||
Medical condition: Up to 60 patients with stable angina pectoris and planned PCI at the University Clinic of Jena are randomly assigned to the glycoprotein IIb/IIIa receptor antagonist abciximab or placebo. Randomisa... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004887-24 | Sponsor Protocol Number: NBK182/1/2020 | Start Date*: 2021-04-14 | |||||||||||
Sponsor Name:Marcin Gruchała Medical University of Gdańsk | |||||||||||||
Full Title: Dual Antithrombotic Therapy with Dabigatran and Ticagrelor in Patients with Acute Coronary Syndrome and Non-valvular Atrial Fibrillation Undergoing Percutaneous Coronary Intervention (ADONIS-PCI) | |||||||||||||
Medical condition: Acute Coronary Syndrome and Non-valvular Atrial Fibrillation Undergoing Percutaneous Coronary Intervention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000191-41 | Sponsor Protocol Number: GC28210 | Start Date*: 2012-06-19 | |||||||||||
Sponsor Name:GENENTECH, Inc. | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY OF THE SAFETY AND EFFICACY OF MPSK3169A IN PATIENTS WITH CORONARY HEART DISEASE OR HIGH RISK OF CORONARY HEART DISEASE | |||||||||||||
Medical condition: Coronary Heart Disease or High Risk of Coronary Heart Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001319-39 | Sponsor Protocol Number: 18/2008/U/Sper | Start Date*: 2008-04-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: PROtection of coronary Microcirculation by Iloprost: Safety and Efficacy in Percutaneous Coronary Intervention | |||||||||||||
Medical condition: Coronary heart disease with stable angina or non-ST elevation myocardial infarction (NSTEMI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001952-20 | Sponsor Protocol Number: NCT:01555658 | Start Date*: 2012-12-14 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: BIVALIRUDIN PLUS STENTING IN lONG LESION TO AVOID PERIPROCEDURAL MYOCARDIAL NECROSIS TRIAL. BILLION TRIAL | |||||||||||||
Medical condition: patients with coronary artery disease after stent implantation in coronary long lesions (>25 mm) and undergoing non urgent percutaneous coronary intervention. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004962-21 | Sponsor Protocol Number: MC-ACS01-2020 | Start Date*: 2021-07-18 | ||||||||||||||||||||||||||
Sponsor Name:Wojskowy Instytut Medyczny | ||||||||||||||||||||||||||||
Full Title: "MetCool ACS”- Metformin “Cooling” Effect on metformin-naive Patients Treated with PCI because of Acute Coronary Syndrome | ||||||||||||||||||||||||||||
Medical condition: Acute coronary syndrome | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001674-80 | Sponsor Protocol Number: ARG-E04 | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:Mitsubishi Pharma Corporation | |||||||||||||
Full Title: A Randomised, Open, Parallel Group, Multicentre Study to Examine the Safety and Effectiveness of Three Doses of Argatroban as Anticoagulant in Combination with Clopidogrel and Aspirin in Patients u... | |||||||||||||
Medical condition: Stable coronary artery disease (CAD) or unstable angina (troponin negative, i.e. within the normal range for the study site) with low to moderate anatomic risk and a requirement for elective percut... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001384-23 | Sponsor Protocol Number: REG1-CLIN310 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Regado Biosciences, Inc. | |||||||||||||
Full Title: A RANDOMIZED, OPEN-LABEL, MULTI-CENTER, ACTIVE-CONTROLLED, PARALLEL GROUP STUDY TO DETERMINE THE EFFICACY AND SAFETY OF THE REG1 ANTICOAGULATION SYSTEM COMPARED TO BIVALIRUDIN IN PATIENTS UNDERGOIN... | |||||||||||||
Medical condition: Coronary Artery Disease (CAD) in patients undergoing Percutaneous Coronary Intervention (PCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) EE (Prematurely Ended) DE (Prematurely Ended) NL (Completed) PT (Prematurely Ended) AT (Completed) GB (Completed) IT (Prematurely Ended) BE (Completed) SK (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) PL (Prematurely Ended) CZ (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004874-14 | Sponsor Protocol Number: 2007-08-16 REPAIR-ACS | Start Date*: 2008-06-09 |
Sponsor Name:Cardiology, J. W. Goethe University Frankfurt | ||
Full Title: Doppel-blinde, randomisierte, kontrollierte Studie zur Erfassung des Effektes einer intrakoronaren Applikation von Knochenmark-Progenitorzellen auf die koronare Flußreserve bei Patienten mit akutem... | ||
Medical condition: Patients with acute coronary syndrome (NSTEMI) due to coronary artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003521-42 | Sponsor Protocol Number: ARG-E08 | Start Date*: 2017-02-09 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma GmbH | |||||||||||||
Full Title: SAICoDis – Safety of Argatroban Infusion in Conduction Disturbances. A prospective, open, multicenter safety study to investigate conduction disturbances in patients receiving argatroban therapy. | |||||||||||||
Medical condition: Patients without diagnosed HIT II but with a coronary heart disease and with a diagnosed stable or unstable angina are planned for a percutaneous coronary intervention (PCI) according to clinical r... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002226-79 | Sponsor Protocol Number: AUGEAS | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Region Skåne | ||||||||||||||||||||||||||||
Full Title: A 30-day, randomized, evalUator-blind, controlled, multi-centre, parallel Group, phase III study to evaluate the Effect of a Low Maintenance Dose TicAgrelor Regimen versus Standard Dose Clopidogrel... | ||||||||||||||||||||||||||||
Medical condition: Coronary Artery Disease (CAD) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005568-40 | Sponsor Protocol Number: LoDoCo2 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:Werkgroep Cardiologische centra Nederland | |||||||||||||
Full Title: Low-dose colchicine for secondary prevention of cardiovascular disease | |||||||||||||
Medical condition: cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003201-26 | Sponsor Protocol Number: 1160.186 | Start Date*: 2014-07-21 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim AB | ||||||||||||||||||
Full Title: A prospective Randomised, open label, blinded endpoint (PROBE) study to Evaluate DUAL antithrombotic therapy with dabigatran etexilate (110mg and 150mg b.i.d.) plus clopidogrel or ticagrelor vs. tr... | ||||||||||||||||||
Medical condition: Patients with non valvular atrial fibrillation (NVAF) that have undergone a percutaneous coronary intervention (PCI) with stenting | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DK (Completed) GR (Completed) DE (Completed) PT (Completed) HU (Completed) ES (Completed) FI (Completed) NL (Completed) CZ (Completed) AT (Completed) IT (Completed) BE (Completed) IE (Completed) SK (Completed) SI (Completed) GB (Completed) BG (Completed) HR (Completed) PL (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000023-15 | Sponsor Protocol Number: H7T-MC-TAAL | Start Date*: 2005-02-10 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: A Comparison of CS-747 and Clopidogrel in Acute Coronary Syndrome Subjects who are to Undergo Percutaneous Coronary Intervention | |||||||||||||
Medical condition: Reduction of atherothrombotic events in patients with acute coronary syndromes (ACS) that is patients with ST-segment elevation MI [STEMI], non-ST-segment elevation MI [NSTEMI], or unstable angina... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) AT (Completed) FI (Completed) HU (Completed) CZ (Completed) SK (Completed) DE (Completed) IT (Completed) LT (Completed) EE (Completed) LV (Completed) IS (Completed) ES (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000952-26 | Sponsor Protocol Number: | Start Date*: 2014-08-19 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: Dual Antiplatelet Therapy to Inhibit Coronary Atherosclerosis and Myocardial Injury in Patients with Necrotic High-risk Coronary Plaque Disease | |||||||||||||
Medical condition: Stable coronary artery disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000200-32 | Sponsor Protocol Number: Version 3.0 19 December 2006 | Start Date*: 2007-05-09 |
Sponsor Name:KANEKA coorporation | ||
Full Title: First in Man Feasibility Study with the MAHOROBA Stent | ||
Medical condition: The study will be performed in patients with symptomatic coronary artery disease (chronic stable angina, silent ischemia, and acute coronary syndrome, excluding ST-elevation myocardial infarction) ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024616-33 | Sponsor Protocol Number: TRO40303CLEQ1491-1 | Start Date*: 2011-08-04 | |||||||||||
Sponsor Name:TROPHOS SA | |||||||||||||
Full Title: Phase II, multicenter, randomized, double-blind, placebo controlled study to assess safety and efficacy of TRO40303 for reduction of reperfusion injury in patients undergoing Percutaneous Coronary ... | |||||||||||||
Medical condition: Treatment for cardiac reperfusion injury in patients undergoing PCI( Percutaneous coronary intervention) to treat an AMI (Acute Myocardial Infarction) and to assess safety as well as the ability of... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004000-13 | Sponsor Protocol Number: D356IC00001 | Start Date*: 2008-02-07 |
Sponsor Name:AstraZeneca AB | ||
Full Title: Study of Coronary Atheroma by InTravascular Ultrasound: Effect of Rosuvastatin Versus AtorvastatiN (SATURN): A 104-week, randomized, double-blind, parallel group, multi-center Phase IIIb study comp... | ||
Medical condition: Coronary Atheroma -- The current trial will study patients who have a clinical indication for coronary catheterization and who have coronary artery disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) FR (Completed) IT (Completed) BE (Completed) HU (Completed) ES (Completed) | ||
Trial results: View results |
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