- Trials with a EudraCT protocol (1,416)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (438)
1,416 result(s) found for: Vascular disease.
Displaying page 1 of 71.
EudraCT Number: 2011-005111-91 | Sponsor Protocol Number: RBHP2011LUSSON | Start Date*: 2012-01-19 | |||||||||||
Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2008-004641-29 | Sponsor Protocol Number: VAS07BE | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:VAS VASCULAR INDEPENDENT RESEACH AND EDUCATION EUROPEAN ORGANIZATION. C/O UNIV MILANO. OSP. L. SACCO | |||||||||||||
Full Title: Non profit study of phase II randomized, double blind, placebo controlled, parallel groups, dose-finding trial with 3 different doses of Betaine versus placebo in subjects affected by PAD (Peripher... | |||||||||||||
Medical condition: Leriche-Fontaine stage II PAD presenting symptoms of intermittent claudication | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) SI (Completed) | |||||||||||||
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: 2009-013681-92 | 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: 2006-005399-42 | Sponsor Protocol Number: GJ001 | Start Date*: 2007-04-11 | |||||||||||
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: Improving symptoms of intermittent claudication in patients with erectile dysfunction and peripheral vascular disease: a pilot study assessing the benefit of daily dosing with tadalafil (Cialis) 10... | |||||||||||||
Medical condition: Peripheral vascular disease (PVD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
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: 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: 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: 2008-005759-21 | Sponsor Protocol Number: | Start Date*: 2011-04-21 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Can atorvastatin improve vascular function in women with a history preeclampsia? A Randomised, double-blinded, placebo-controlled crossover trial of atorvastatin in women with a history of preeclam... | |||||||||||||
Medical condition: Cardiovascular disease in women with a history of preeclampsia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005612-40 | Sponsor Protocol Number: DAM/001/08 | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:FARMACEUTICI DAMOR | |||||||||||||
Full Title: Open-label, controlled, randomised, multicentre, parallel group clinical trial of efficacy and tolerability of heparan sulfate slow-release 120 mg tablets and defibrotide 400 mg capsules in the tre... | |||||||||||||
Medical condition: Patients with chronic venous insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000706-37 | Sponsor Protocol Number: CLLG783X2201 | Start Date*: 2017-11-28 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A Patient and Investigator-blinded, randomized, placebo controlled study of LLG783 in patients with peripheral artery disease (PAD) and intermittent claudication. | ||||||||||||||||||
Medical condition: Peripheral Artery Disease (PAD), Intermittent Claudication | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (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: 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: 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: 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: 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 |
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