- Trials with a EudraCT protocol (68)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    68 result(s) found for: Coronary stenting.
                    
                
			
   			
		
		Displaying page 1 of 4.
	
	
	| EudraCT Number: 2011-005305-73 | Sponsor Protocol Number: CTHC1 | Start Date*: 2012-07-06 | |||||||||||
| Sponsor Name:University Medical Center of the Johannes Gutenberg-University Mainz | |||||||||||||
| Full Title: Effects of clopidogrel vs prasugel vs ticagrelor on endothelial function, inflammatory and oxidative stress parameters and platelet function in patients undergoing coronary artery stenting. A rando... | |||||||||||||
| Medical condition: Coronary artery disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000823-11 | Sponsor Protocol Number: TIMO | Start Date*: 2023-03-09 | ||||||||||||||||
| Sponsor Name:Sahlgrenska University Hospital Gothenburg | ||||||||||||||||||
| Full Title: Ticagrelor monotherapy after coronary stenting in patients with acute myocardial infarction. A prospective single-centre, single-arm phase II study | ||||||||||||||||||
| Medical condition: Antiplatelet therapy in patients who undergo coronary artery stenting due to coronary artery disease (CAD) or acute coronary syndrome (ACS). The present study will examine whether ticagrelor, as mo... | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| 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: 2004-000517-19 | Sponsor Protocol Number: 00/04/02 | Start Date*: 2005-11-23 | 
| Sponsor Name:Blackpool Fylde & Wyre Healthcare NHS Trust | ||
| Full Title: PRETREATMENT WITH HIGH DOSE CLOPIDOGREL FOR REDUCTION OF THROMBOTIC EVENTS AFTER ELECTIVE CORONARY TERRITORY STENTING WITH DRUG ELUTING STENTS: ThePROTECTED Study | ||
| Medical condition: PERCUTANEOUS CORONARY INTERVENTION( USING DRUG ELUTING STENTS) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| 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: 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: 2007-006263-68 | 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: 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: 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: 2006-000770-75 | Sponsor Protocol Number: CE 14/05 CEREA-DES | Start Date*: 2005-11-01 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA | |||||||||||||
| Full Title: Cortisone Eliminates Restenosis as Effectively As DES | |||||||||||||
| Medical condition: To assess the clinical efficacy and safety of the prednisone therapy after PCI as a low-tech low-cost systemic alternative to currently available BMS and DES. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003518-41 | Sponsor Protocol Number: 2018-4765 | Start Date*: 2019-10-03 | 
| Sponsor Name:Radboudumc | ||
| Full Title: Efficacy of Diltiazem to improve coronary microvascular dysfunction: A randomized clinical trial | ||
| Medical condition: Coronary Microvascular Dysfunction (CMD). In CMD, ischemia is caused by impaired endothelial and/or non-endothelial coronary vasoreactivity resulting in the coronary microvasculature not dilating p... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-002617-39 | Sponsor Protocol Number: Fondazione Mediolanum 001/2007 | Start Date*: 2008-01-23 | |||||||||||
| Sponsor Name:Fondazione Mediolanum Onlus | |||||||||||||
| Full Title: INtegrilin plus STenting to Avoid Myocardial Necrosis Trial | |||||||||||||
| Medical condition: Patients with diffuse CAD undergoing percutaneous treatment on a native coronary vessel with planned implantation of two DES in overlapping with a total stent length 33 mm for diffuse coronary dis... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004446-42 | Sponsor Protocol Number: MB11-2018 | Start Date*: 2019-06-20 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S.CROCE E CARLE CUNEO | |||||||||||||
| Full Title: Maintenance Of aNtiplatElet Therapy in patients with coronary stenting undergoing surgery | |||||||||||||
| Medical condition: Patients a least 18 years of age on DAPT per standard of care who are planned to undergo non deferrable cardiac and non cardiac surgery which will require discontinuation of a P2Y12 inhibitor. Subj... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003684-32 | Sponsor Protocol Number: ISTANT | Start Date*: 2008-06-18 | |||||||||||
| Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
| Full Title: Integrilin plus stenting to avoid myocardial necrosis trial. Pilot Study | |||||||||||||
| Medical condition: patients with diffuse CAD undergoing percutaneous treatment on a native coronary vassel with planned implantation of 33 mm of DES with reference vessel diameter 2.25-4.0 mm. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003621-33 | Sponsor Protocol Number: ESR-15-10793 | Start Date*: 2016-02-25 | |||||||||||
| Sponsor Name:Fundación Interhospitalaria de Investigación Cardiovascular | |||||||||||||
| Full Title: PRotective Effect on the coronary microcirculation of patients with DIabetes by Clopidogrel or Ticagrelor:A randomized multicenter clinical trial using intracoronary multimodal physiology | |||||||||||||
| Medical condition: Ischemic Heart Disease in Diabetic patients | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| 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) | |||||||||||||
| 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: 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: 2008-003839-20 | Sponsor Protocol Number: CVT5127 | Start Date*: 2009-02-24 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Open-Label, Parallel-Group, Exploratory Study to Evaluate the Efficacy and Safety of 400 µg Regadenoson Bolus for Pharmacological Stress Echocardiography | |||||||||||||
| Medical condition: Suspected coronary artery disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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