- Trials with a EudraCT protocol (169)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
169 result(s) found for: Coronary stent.
Displaying page 1 of 9.
EudraCT Number: 2005-001481-14 | Sponsor Protocol Number: TAX-001 | Start Date*: 2005-06-22 |
Sponsor Name:University Hospital Tübingen | ||
Full Title: LOCAL-TAX Trial: Local intracoronary administration of Paclitaxel after stent implantation for prevention of restenosis in comparison with stent implantation alone and with implantation of a Paclit... | ||
Medical condition: coronary heart disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001148-40 | Sponsor Protocol Number: ExcelsiorLOAD | Start Date*: 2014-06-02 | |||||||||||||||||||||
Sponsor Name:Heart Center Freiburg - Bad Krozingen | |||||||||||||||||||||||
Full Title: Pharmacodynamic comparison of thienopyridine loading strategies in patients undergoing elective coronary stenting | |||||||||||||||||||||||
Medical condition: Stable patients with obstructive coronary heart disease undergoing elective percutaneous coronary stent implantation. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005071-25 | Sponsor Protocol Number: ExcelsiorLOAD2 | Start Date*: 2016-01-19 | |||||||||||||||||||||
Sponsor Name:University Heart Center Freiburg - Bad Krozingen | |||||||||||||||||||||||
Full Title: Pharmacodynamic comparison of different oral P2Y12-receptor inhibitor loading strategies for transitioning from cangrelor in patients undergoing coronary stenting | |||||||||||||||||||||||
Medical condition: Patients with obstructive coronary heart disease undergoing percutaneous coronary stent implantation. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006481-42 | Sponsor Protocol Number: 769 | Start Date*: 2007-01-16 | |||||||||||
Sponsor Name:Orbus International BV | |||||||||||||
Full Title: HEALING IIB - Healthy Endothelial Accelerated Lining Inhibits Neointimal Growth A Clinical, Multi-center, Prospective, non-Randomized Study | |||||||||||||
Medical condition: Patients with ischemic hear disease with up to two de novo native coronary artery lesions. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001540-31 | Sponsor Protocol Number: 05EU01 | Start Date*: 2006-11-09 |
Sponsor Name:BIOSENSORS EUROPE SA | ||
Full Title: LIMUS ELUTED FROM A DURABLE VERSUS ERODABLE STENT COATING | ||
Medical condition: Coronary heart disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006263-68 | Sponsor Protocol Number: GEIDENo.A01207 | Start Date*: 2008-07-24 | |||||||||||
Sponsor Name:Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen | |||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF 6 MONTHS VERSUS 12 MONTHS CLOPIDOGREL THERAPY AFTER IMPLANTATION OF A DRUG-ELUTING STENT SAFETY AND EFFICACY OF SIX MONTHS DUAL ANTIPLATELET ... | |||||||||||||
Medical condition: Patients with established coronary artery disease on chronic clopidogrel therapy at 6 months after coronary drug eluting stent implantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004783-38 | Sponsor Protocol Number: STH18423 | Start Date*: 2015-02-04 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Study of two regimens of TicagrElor compared to clopidogrel in patients undergoing ELective Percutaneous Coronary Intervention (STEEL PCI) | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000713-35 | Sponsor Protocol Number: AVI-4126-17 | Start Date*: 2005-08-08 |
Sponsor Name:AVI BioPharma Inc. | ||
Full Title: A Phase IIA Study to Evaluate the Safety and Preliminary Efficacy of Resten-MP when used in Conjunction with a Bare Metal Stent in de novo Native Coronary Artery Lesions | ||
Medical condition: Coronary Artery Stenosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005491-27 | Sponsor Protocol Number: U-08-002 | Start Date*: 2008-11-26 | |||||||||||
Sponsor Name:UCR Uppsala Clinical Research Center | |||||||||||||
Full Title: TAILORING OF PLATELET INHIBITION TO AVOID STENT THROMBOSIS TOPAS-1 A Pharmacodynamic Phase II Study of Clopidogrel P2Y12 Platelet Inhibition | |||||||||||||
Medical condition: Previous patients in the TABR study treated with Plavix 75 mg/day and patients with stent thrombosis within 6 months or myocardial infarction within 6 month after stenting. For the control group no... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (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: 2007-001794-28 | Sponsor Protocol Number: 806 | Start Date*: 2007-10-15 | |||||||||||
Sponsor Name:OrbusNeich Medical BV | |||||||||||||
Full Title: Endothelial Function following stenting with Genous vs Drug-Eluting Stents | |||||||||||||
Medical condition: Patients with symptomatic ischemic heart disease expressing one or two de novo native coronary artery lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004510-99 | Sponsor Protocol Number: 012017POEM | Start Date*: 2017-02-21 | |||||||||||
Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: PERFORMANCE OF BIORESORBABLE POLYMER-COATED EVEROLIMUS-ELUTING SYNERGY® STENT IN PATIENTS AT HIGH BLEEDING RISK UNDERGOING PERCUTANEOUS CORONARY REVASCULARIZATION FOLLOWED BY 1-MONTH DUAL ANTIPLATE... | |||||||||||||
Medical condition: Coronary artery disease with high-bleeding risk (HBR) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003515-58 | Sponsor Protocol Number: ECRI-12-001 | Start Date*: 2013-05-25 | |||||||||||
Sponsor Name:ECRI | |||||||||||||
Full Title: GLOBAL LEADERS: Comparative effectiveness of 1 month of ticagrelor plus aspirin followed by ticagrelor monotherapy versus a current-day intensive dual antiplatelet therapy in all-comers patients un... | |||||||||||||
Medical condition: Subjects either male or female eligible for percutaneous coronary intervention (PCI) with lesions suitable for stent implantation who meet all eligibility criteria and provide written informed cons... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GB (Completed) AT (Completed) ES (Completed) BE (Completed) NL (Completed) DK (Completed) HU (Completed) PT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012206-39 | Sponsor Protocol Number: ALX-0081-2.1/09 | Start Date*: 2009-08-14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Ablynx | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase II randomized, open label clinical trial in high risk percutaneous coronary intervention (PCI) patients receiving standard antithrombotic treatment plus either ALX-0081 or GPIIb/IIIa inhibi... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Thrombotic events associated with percutaneous coronary intervention (PCI) in patients with unstable angina or Non ST-Segment Elevation Myocardial Infarction (NSTEMI), or stable angina with at leas... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) AT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003026-14 | Sponsor Protocol Number: PREVENTBURDEN | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:KA Rudolfstiftung - 2. Medizinische Abteilung | |||||||||||||
Full Title: | |||||||||||||
Medical condition: coronary artery disease with a single coronary vessel requiring stent implantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004376-35 | Sponsor Protocol Number: ISSBRILO176 | Start Date*: 2014-01-14 | |||||||||||
Sponsor Name:Hellenic Cardiovascular Research Society | |||||||||||||
Full Title: A Single Center, Phase II, Assessor-Blinded, RaNdomized, Active Controlled, Parallel-Group Trial to COmpare Ticagrelor Versus Clopidogrel on the REduction of ArteriaL STiffness and Wave Reflections... | |||||||||||||
Medical condition: Coronary Artery Disease (with an indication for coronary angiography) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000192-14 | Sponsor Protocol Number: TMC-CAN-05-02 | Start Date*: 2006-12-21 | |||||||||||
Sponsor Name:The Medicines Company | |||||||||||||
Full Title: A Clinical Trial Comparing Cangrelor To Clopidogrel In Subjects Who Require Percutaneous Coronary Intervention | |||||||||||||
Medical condition: Subjects with coronary atherosclerosis who require PCI (with or without stent). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Completed) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000583-96 | Sponsor Protocol Number: 2011-000583-96 | Start Date*: 2011-08-05 | |||||||||||
Sponsor Name:Aarhus University Hospital, Skejby | |||||||||||||
Full Title: Undersøgelse af 6-uger versus 6-måneders clopidogrel behandling hos patienter med samtidig aspirin og oral angikoagulans behandling efter implantation af en drug-eluting stent | |||||||||||||
Medical condition: Patients with coronary artery disease and ongoing treatment with an oral anticoagulant agent (warfarin), who have indication for treatment with a drug-eluting stent and therefore have indication fo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003906-34 | Sponsor Protocol Number: ANGIODAPT-01 | Start Date*: 2023-02-24 | |||||||||||
Sponsor Name:iVascular, S.L.U. | |||||||||||||
Full Title: Ischemic and bleeding outcomes after angiolite stent implantation and an abbreviated dual antiplatelet therapy. A 2x2 factorial, all-comer, multicenter, randomized controlled trial: Angiodapt. | |||||||||||||
Medical condition: Coronary artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015712-17 | Sponsor Protocol Number: G080186 | Start Date*: 2010-03-25 | |||||||||||
Sponsor Name:HCRI | |||||||||||||
Full Title: A prospective, multi-center, randomized, double-blind trial to assess the effectiveness and safety of 12 versus 30 months of dual antiplatelet therapy (DAPT) in subjects undergoing percutaneous cor... | |||||||||||||
Medical condition: Dual antiplatelet therapy (DAPT) in subjects undergoing percutaneous coronary intervention (PCI) with either drug eluting stent (DES) or bara metal stent (BMS) placement for the treatment of corona... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) DE (Completed) CZ (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
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