- Trials with a EudraCT protocol (125)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
125 result(s) found for: Ankle brachial index.
Displaying page 1 of 7.
EudraCT Number: 2010-024391-25 | Sponsor Protocol Number: 2010CLI01 | Start Date*: 2011-05-11 |
Sponsor Name:XCell-Center GmbH | ||
Full Title: A Multi-centre, double blind, randomized placebo controlled phase II study to assess the efficacy and safety of ASCT01 in Critical limb Ischemia Patients - SCILI | ||
Medical condition: Critical Limb Ischemia Rutherford clas 4-6 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2013-004342-42 | Sponsor Protocol Number: 201302 | Start Date*: 2014-03-26 | |||||||||||
Sponsor Name:Medisch Centrum Alkmaar | |||||||||||||
Full Title: The effect of fish oil supplements on hemorheological parameters and walking distance in patients with intermittent claudication | |||||||||||||
Medical condition: Patients suffering from intermittent claudication | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018190-31 | Sponsor Protocol Number: V1.0,14.12.2009 | Start Date*: 2010-08-03 |
Sponsor Name:Medizinische Universität Wien, Univ.Klinik f.Innere Medizin II, Abt.f.Angiologie | ||
Full Title: OMEGA-3-POLYUNSATURATED FATTY-ACIDS (n3-PUFA) IN PATIENTS WITH PERIPHERAL ARTERIAL DISEASE: EFFECTS ON ENDOTHELIAL FUNCTION – A RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND TRIAL | ||
Medical condition: peripheral arterial disease (PAD) and intermittent claudication (IC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001800-20 | Sponsor Protocol Number: PADBelch07 | Start Date*: 2007-08-10 |
Sponsor Name:University of Dundee | ||
Full Title: A randomised, placebo-controlled trial of the effect of pioglitazone on vascular endothelial function and novel biomarkers for macrovascular events in diabetics with established peripheral arterial... | ||
Medical condition: The study involves patients with type 2 Diabetes and Peripheral Arterial Disease.The overall objective of the research proposal is to determine the occurrence of biomarkers that typify the metaboli... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000434-34 | Sponsor Protocol Number: UMCU-VASC-CO-003 | Start Date*: 2023-04-12 |
Sponsor Name:University Medical Centre Utrecht | ||
Full Title: A placebo-controlled, double-blind randomized trial evaluating the effect of etidronate in young patients with pseudoxanthoma elasticum on ectopic mineralization. | ||
Medical condition: Pseudoxanthoma elasticum | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016600-23 | Sponsor Protocol Number: 05102009 | Start Date*: 2010-07-09 |
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||
Full Title: A double blind, randomised, placebo controlled trial to study the clinical effectiveness of Angiotensin Converting Enzyme (ACE) inhibitors, ramipril,in patients with intermittent claudication | ||
Medical condition: Intermittent Claudication | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-003399-38 | Sponsor Protocol Number: NN9535-4533 | Start Date*: 2020-08-28 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Effects of semaglutide on functional capacity in patients with type 2 diabetes and peripheral arterial disease | |||||||||||||
Medical condition: Peripheral arterial disease Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) HU (Completed) NO (Completed) BE (Completed) DK (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001538-15 | Sponsor Protocol Number: 6034 | Start Date*: 2007-06-12 |
Sponsor Name:Sangart Inc | ||
Full Title: A randomized, single-blind, controlled Phase II pilot study of Hemospan® compared with colloid (Voluven®) to evaluate vascular resistance and blood flow in the forearm, and to assess local skin blo... | ||
Medical condition: chronic critical limb ischemia (CCLI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003915-30 | Sponsor Protocol Number: MT4VLU07/A-V7 | Start Date*: 2008-05-15 |
Sponsor Name:Gloucestershire Hospitals NHS Foundation Trust | ||
Full Title: The efficacy of maggots as a debridement agent for venous leg ulcers | ||
Medical condition: The purpose of the trial is to evaluate the effectiveness of BioFOAM maggots in achieving rapid debridement of chronic venous leg ulcers. Removal of slough and necrotic tissue from these wounds is ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004863-32 | Sponsor Protocol Number: BCBE/04/NEB-PAO/087 | Start Date*: 2006-03-08 |
Sponsor Name:Berlin-Chemie Menarini | ||
Full Title: EFFECTS OF NEBIVOLOL ON THE WALKING ABILITY IN PATIENTS WITH ESSENTIAL HYPERTENSION AND PERIPHERAL ARTERIAL DISEASE INTERMITTENT CLAUDICATION | ||
Medical condition: ESSENTIAL HYPERTENSION AND PERIPHERAL ARTERIAL DISEASE INTERMITTENT CLAUDICATION | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002327-13 | Sponsor Protocol Number: 2004VS002 | Start Date*: 2005-07-01 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: Mild to moderate intermittent claudication: the clinical and cost-effectiveness of supervised exercise programmes and Cilostazol therapy in patient management | ||
Medical condition: Intermittent claudication | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003818-26 | Sponsor Protocol Number: K-877-302 | Start Date*: 2017-03-16 | |||||||||||
Sponsor Name:Kowa Research Institute, Inc. | |||||||||||||
Full Title: Pemafibrate to Reduce cardiovascular OutcoMes by reducing triglycerides IN patiENts with diabeTes (PROMINENT) | |||||||||||||
Medical condition: Reduction of cardiovascular events in patients with Type II Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) NL (Prematurely Ended) BG (Prematurely Ended) DE (Completed) DK (Completed) GB (GB - no longer in EU/EEA) ES (Prematurely Ended) HU (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006719-20 | Sponsor Protocol Number: 0431-082 | Start Date*: 2009-05-27 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co. | |||||||||||||
Full Title: TECOS: A Randomized, Placebo Controlled Clinical Trial to Evaluate Cardiovascular Outcomes after Treatment with Sitagliptin in Patients with Type 2 Diabetes Mellitus and Inadequate Glycemic Control | |||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) NL (Completed) DE (Completed) ES (Completed) HU (Completed) LV (Completed) FR (Completed) CZ (Completed) GB (Completed) IE (Prematurely Ended) SK (Completed) BG (Completed) IT (Completed) EE (Completed) FI (Completed) SE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010062-33 | Sponsor Protocol Number: ABH-DERMAGRAFT-001-08 | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:Advanced BioHealing Inc | |||||||||||||
Full Title: A Prospective, Multi-center, Randomized, Controlled Clinical Investigation of Dermagraft® in Subjects with Venous Leg Ulcers | |||||||||||||
Medical condition: Venous leg ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) EE (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000822-58 | Sponsor Protocol Number: C9253 | Start Date*: 2004-07-13 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Groupe | |||||||||||||
Full Title: A double blind randomized study of Clopidogrel 75 mg/d versus placebo on a background of ASA 75-100 mg/d, in peripheral disease (PAD) patient receiving a unilateral below knee by-pass graft. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) HU (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004853-59 | Sponsor Protocol Number: EX6018-4758 | Start Date*: 2021-08-16 | ||||||||||||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||||||||||||
Full Title: ZEUS - Effects of ziltivekimab versus placebo on cardiovascular outcomes in participants with established atherosclerotic cardiovascular disease, chronic kidney disease and systemic inflammation | ||||||||||||||||||||||||||||
Medical condition: Atherosclerotic cardiovascular disease Chronic kidney disease Systemic inflammation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: LT (Trial now transitioned) SK (Trial now transitioned) DE (Trial now transitioned) NL (Ongoing) SE (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) BG (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) LV (Trial now transitioned) HR (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002467-26 | Sponsor Protocol Number: 480-SFA2013-001 | Start Date*: 2013-08-30 |
Sponsor Name:480 Biomedical, Inc. | ||
Full Title: The SPRINT trial: An Evaluation of the 480 Biomedical STANZA™ Drug-Eluting Resorbable Scaffold (DRS) System v1.2 in the Treatment of de novo SFA Lesions | ||
Medical condition: An evaluation of the safety and performance of the STANZA DRS v1.2 system for the treatment of patients with obstructive superficial femoral artery disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002942-20 | Sponsor Protocol Number: EFC5826 | Start Date*: 2005-12-29 | |||||||||||
Sponsor Name:sanofi-aventis recherche et developpement | |||||||||||||
Full Title: Randomized, multinational, multicenter, double-blind, placebo-controlled, two-arm parallel group trial of rimonabant 20 mg OD for reducing the risk of major cardiovascular events in abdominally obe... | |||||||||||||
Medical condition: Patients with abdominal obesity at increased risk for cardiovascular events (myocardial infarctio, stroke and cardiovascular death) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prohibited by CA) GB (Prematurely Ended) ES (Completed) DE (Completed) AT (Prematurely Ended) FI (Completed) BE (Completed) DK (Suspended by CA) HU (Completed) CZ (Suspended by CA) IE (Prematurely Ended) PT (Completed) GR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004913-11 | Sponsor Protocol Number: 111075 | Start Date*: 2021-02-18 |
Sponsor Name:Radboudumc | ||
Full Title: genotype-guided strategy for antithrombotic treatment versus conventional clopidogrel therapy in peripheral arterial disease’ | ||
Medical condition: Symptomatic or stable pheripheral artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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