- Trials with a EudraCT protocol (466)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    466 result(s) found for: Vascular system.
                    
                
			
   			
		
		Displaying page 1 of 24.
	
	
	| EudraCT Number: 2008-005006-39 | Sponsor Protocol Number: selene 2008 | Start Date*: 2009-02-24 | ||||||||||||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PISANA | ||||||||||||||||||||||||||||
| Full Title: Study on the vascular effects of ACE-I + CA-antagonist (Enalapril + Lercanidipine) versus ACE-I + diuretic (Enalapril + hydrochlorothiazidE) combinations in hypertensive patients with metabolic syn... | ||||||||||||||||||||||||||||
| Medical condition: hypertensive patients of either sex aged 40-69 years | ||||||||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2009-013681-92 | Sponsor Protocol Number: PREVENT-ICARUS V1 | Start Date*: 2009-10-29 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
| Full Title: PRevEntion of cardiac and Vascular pEriprocedural complications in patients undergoiNg coronary angiography or angioplasTy: IntraCoronary Adenosine administration to prevent peRiprocedUral myonecro... | |||||||||||||
| Medical condition: Elective coronary angioplasty | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006304-38 | Sponsor Protocol Number: 1381/08 | Start Date*: 2008-12-23 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Protocol for a study on male patients suffering from peripheral arterial disease with severe chronic limb ischemia during treatment with iloprost: assessment of oxidative stress and organic erectil... | |||||||||||||
| Medical condition: peripheral arterial disease and organic erectile dysfunction. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017640-13 | Sponsor Protocol Number: Blocchi09 | Start Date*: 2010-04-21 | |||||||||||
| Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
| Full Title: Continuous peripheral block in the pain and ischemic ulcer treatment in arteriopathy patients | |||||||||||||
| Medical condition: Arteriophaty patients with ischemic pain and/or ulcers | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017448-15 | Sponsor Protocol Number: GAIN | Start Date*: 2009-12-15 | |||||||||||
| Sponsor Name:ISTITUTO NEUROLOGICO MEDITERRANEO NEUROMED | |||||||||||||
| Full Title: A multicenter, open label, hystorical Group controlled study by evaluate the effectivness and sAfety in the use of INfliximab (Tumor necrosis factor - alfa antibody) in preventing or reducing cereb... | |||||||||||||
| Medical condition: patient with cerebral hemorrhage | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001347-21 | Sponsor Protocol Number: EPA 2007 | Start Date*: 2007-03-05 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: A randomised clinical trial on heparin versus saline solution (NaCl 0,9%) in the maintenance of peripherical venous catheters | |||||||||||||
| Medical condition: PVC flow maintenance | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005056-16 | Sponsor Protocol Number: ATORV/IMAPERIPROC | Start Date*: 2007-10-19 | |||||||||||
| Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
| Full Title: Atorvastatin at high dosage before coronary stent surgery: effect on peri-procedure miocardic stroke . | |||||||||||||
| Medical condition: elective PCI in de novo coronaric lesions | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001660-23 | Sponsor Protocol Number: AOCP[1].IIb.Prot.DiSalvo.Mazzone.f | Start Date*: 2007-11-12 | |||||||||||
| Sponsor Name:CENTRO STUDI FADOI | |||||||||||||
| Full Title: Optimized treatment of patients with severe peripheral arterial disease (Leriche-Fontaine stage IIb), when open or endovascular intervention is possible or not, in terms of measurement of pain free... | |||||||||||||
| Medical condition: Arteropatia obliterante cronica periferica | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000966-10 | Sponsor Protocol Number: 38/2004/U/sper | Start Date*: 2004-03-23 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: na | |||||||||||||
| Medical condition: ESSENTIAL HYPERTENSION | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002157-38 | Sponsor Protocol Number: 57911 | Start Date*: 2017-09-14 | ||||||||||||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||||||||||||
| Full Title: Treatment of congenital vascular malformations using Sirolimus: improving quality of Life | ||||||||||||||||||||||||||||
| Medical condition: congenital vascular malformation : Vascular malformations can involve lymphatic vessels, capillaries, veins and arteries or even combinations. These vascular malformations are present at birth an... | ||||||||||||||||||||||||||||
					
						
							
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| Population Age: Infants and toddlers, Children, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-005330-18 | Sponsor Protocol Number: ARMYDA_CAROTID | Start Date*: 2011-11-08 | |||||||||||
| Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
| Full Title: Prospective randomized study to evaluate the efficacy of different protocols IN DRUG PREVENTION OF BRAIN DAMAGE AFTER Carotid angioplasty with stent implantation (CAROTID ARMYDA trial). | |||||||||||||
| Medical condition: Patients with carotid stenosis undergoing angioplasty with stent implantation | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003627-29 | Sponsor Protocol Number: PREVENTIHSSTUDY(FARM12L9JE) | Start Date*: 2017-02-22 | |||||||||||
| Sponsor Name:OSPEDALE SANTA MARIA DELLA MISERICORDIA | |||||||||||||
| Full Title: PREvention of VENous Thromboembolism In Hemorrhagic Stroke patients | |||||||||||||
| Medical condition: hemorrhagic stroke | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000868-15 | Sponsor Protocol Number: PENT_PTA | Start Date*: 2012-03-06 | |||||||||||
| Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
| Full Title: EFFECT OF TREATMENT WITH PENTOXIFYLLINE ABOUT THE RISK RATER OF POST-angioplasty restenosis IN PATIENTS WITH LOWER LIMB arterial disease | |||||||||||||
| Medical condition: PERIPHERAL ARTERIOPATHY | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004583-22 | Sponsor Protocol Number: 548.12 | Start Date*: 2012-10-20 | |||||||||||
| Sponsor Name:OSPEDALE PEDIATRICO BAMBINO GESU' DI ROMA | |||||||||||||
| Full Title: Verification of the effectiveness of intravenous sildenafil compared to other pulmonary vasodilators used in the test vessel reactivity of pulmonary | |||||||||||||
| Medical condition: Subjects in children with congenital heart disease surgery or not, with echocardiographic signs of pulmonary hypertension followed at the Pediatric Cardiology Centre of the Mediterranean or reporte... | |||||||||||||
					
						
							
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| Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002314-21 | Sponsor Protocol Number: MEN IFR/08/NEB-HYP/01 | Start Date*: 2008-05-23 | ||||||||||||||||
| Sponsor Name:A. MENARINI I.F.R. | ||||||||||||||||||
| Full Title: VALUTAZIONE COMPARATIVA DEGLI EFFETTI SULLA FUNZIONE ENDOTELIALE DEL TRATTAMENTO CON NEBIVOLOLO E IDROCLOROTIAZIDE VS IRBESARTAN E IDROCLOROTIAZIDE IN PAZIENTI CON IPERTENSIONE ARTERIOSA NEO-DIAGNO... | ||||||||||||||||||
| Medical condition: IPERTENSIONE ARTERIOSA | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-001635-21 | Sponsor Protocol Number: VIA-2291-02 | Start Date*: 2006-12-21 | |||||||||||
| Sponsor Name:VIA PHARMACEUTICALS, INC. | |||||||||||||
| Full Title: A Phase 2 Randomised, Double-blind, Placebo-controlled Study of the Effects of VIA-2291, a 5-lipoxygenase Inhibitor, on Atherosclerotic Plaque and Biomarkers of Vascular Inflammation in Patients wi... | |||||||||||||
| Medical condition: Carotid Stenosis. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010399-10 | Sponsor Protocol Number: STAT | Start Date*: 2009-04-16 | ||||||||||||||||
| Sponsor Name:OSPEDALE G.PASQUINUCCI-FONDAZIONE G.MONASTERIO | ||||||||||||||||||
| Full Title: STANDARD VERSUS TAILORED ANTI-PLATELET THERAPY IN ACS PATIENTS UNDERGOING PERCUTANEOUS CORONARY ANGIOPLASTY | ||||||||||||||||||
| Medical condition: PATIENTS UNDERGOING CORONARY ANGIOPLASTY FOR ACUTE CORONARY SYNDROME TYPE STEMI / NSTEMI ESC | ||||||||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-004146-41 | Sponsor Protocol Number: 49RC18_0197 | Start Date*: 2019-01-30 | |||||||||||||||||||||||||||||||
| Sponsor Name:CHU Angers | |||||||||||||||||||||||||||||||||
| Full Title: First-BLINDOS - Evaluation d’une stratégie de dépistage systématique de la carence en vitamine D et du traitement en cas de déficit, sur l’amélioration de la distance maximale de marche chez les pa... | |||||||||||||||||||||||||||||||||
| Medical condition: Artériopathie oblitérante des membres inférieurs de stade 2 | |||||||||||||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-007516-15 | Sponsor Protocol Number: HEP/NEB082000N/NEB4.01 | Start Date*: 2009-02-02 | ||||||||||||||||
| Sponsor Name:Laboratoires NEGMA | ||||||||||||||||||
| Full Title: Comparaison des effets du nébivolol et de l'aténolol sur la fonction endothéliale vasomotrice des artères de conductance lors de l'hypertension artérielle essentielle | ||||||||||||||||||
| Medical condition: Hypertension artérielle | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-005720-15 | Sponsor Protocol Number: CLZC696A2224 | Start Date*: 2013-09-11 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A randomized, double-blind, active-controlled, parallel group, 52-week study to evaluate the effect of LCZ696 compared to olmesartan on regional aortic stiffness in subjects with essential hyperten... | ||||||||||||||||||
| Medical condition: Hypertensive patients. | ||||||||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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