- Trials with a EudraCT protocol (329)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
329 result(s) found for: Peripheral Vascular Disease.
Displaying page 1 of 17.
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: 2008-004641-29 | 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: 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: 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: 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: 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: 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: 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: 2014-005569-58 | Sponsor Protocol Number: BAY59-7939/17454 | Start Date*: 2015-09-23 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: An international, multicenter, randomized, double-blind, placebo-controlled phase 3 trial investigating the efficacy and safety of Rivaroxaban to reduce the risk of major thrombotic vascular event... | |||||||||||||
Medical condition: Peripheral artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) ES (Completed) HU (Completed) GB (Completed) FR (Completed) PT (Completed) SE (Completed) BE (Completed) BG (Completed) DK (Completed) DE (Completed) NL (Completed) PL (Completed) SK (Completed) LT (Completed) LV (Completed) RO (Completed) EE (Completed) FI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004762-40 | Sponsor Protocol Number: Rosudip01 | Start Date*: 2007-10-18 | |||||||||||
Sponsor Name:Dept. Pharmacology and Toxicology | |||||||||||||
Full Title: Rosuvastatin augments dipyridamole induced vasodilation by increased adenosine receptor stimulation | |||||||||||||
Medical condition: Ischemia-reperfusion injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002520-16 | Sponsor Protocol Number: 626 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:Universitätsklinik für klinische Pharmakologie, Medizinische Universität Wien | |||||||||||||
Full Title: The effects of post-conditioning and administration of Vitamin C on intramuscular high energy phosphate levels | |||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003652-35 | Sponsor Protocol Number: 300 | Start Date*: 2006-02-02 |
Sponsor Name:Barnsley Hospital NHS Foundation Trust | ||
Full Title: A randomised, double blind, placebo controlled study to assess the effect of testosterone treatment on arterial stiffness in patients with type 2 diabetes, peripheral vascular disease and hypogonad... | ||
Medical condition: Male Hypogonadism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001162-40 | Sponsor Protocol Number: E2020-A001-233 | Start Date*: 2005-03-08 | |||||||||||
Sponsor Name:Eisai Ltd | |||||||||||||
Full Title: An 18-week, multi-center, randomized, double-blind, placebo-controlled, parallel-group study of the efficacy, safety, and tolerability of donepezil HCl (E2020) in patients with CADASIL who have cog... | |||||||||||||
Medical condition: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). CADASIL is a genetic disorder representing a minority of the patients who develop vascular de... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Completed) SE (Completed) GB (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001397-15 | Sponsor Protocol Number: BMMNC_CLI_001 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
Full Title: A prospective, randomized study to compare the effect on tissue oxygenation and clinical outcome of autologous bone marrow-derived mononuclear cell therapy with standard treatment in patients with ... | |||||||||||||
Medical condition: Autologous cell therapy (ACT) is new technique for patients with critical limb ischemia and diabetic foot (DF). In our study, the effect of ACT and also the repetitive treatment will be compared wi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004616-36 | Sponsor Protocol Number: D5135C00001 | Start Date*: 2013-02-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomized, double-blind, parallel group, multicentre phase IIIb study to compare ticagrelor with clopidogrel treatment on the risk of cardiovascular death, myocardial infarction and ischemic str... | |||||||||||||
Medical condition: peripheral artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) NL (Completed) PL (Completed) GB (Completed) SE (Completed) ES (Completed) DE (Completed) HU (Completed) BG (Completed) CZ (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002228-34 | Sponsor Protocol Number: 2012/1vas | Start Date*: 2015-09-30 | |||||||||||||||||||||
Sponsor Name:Diego Caicedo Valdés | |||||||||||||||||||||||
Full Title: Growth hormone (GH) angiogenic effect clinical trial on patients with lower limb critical ischemia. GHAS Study | |||||||||||||||||||||||
Medical condition: Lower limb critical ischemia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001491-11 | Sponsor Protocol Number: EV01 | Start Date*: 2020-07-24 | |||||||||||||||||||||
Sponsor Name:IRCCS SAN RAFFAELE PISANA GESTITO DA SAN RAFFAELE ROMA SRL | |||||||||||||||||||||||
Full Title: Phase IV study for efficacy and safety of Evolocumab added to Ezetimibe (Standard of Care) in high cardiovascular risk haemodialized statin intolerant patients with hypercholesterolemia. | |||||||||||||||||||||||
Medical condition: High cardiovascular risk haemodialized statin intolerant patients with hypercholesterolemia. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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