- Trials with a EudraCT protocol (1,302)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,302 result(s) found for: Vascular diseases.
Displaying page 5 of 66.
EudraCT Number: 2015-001953-33 | Sponsor Protocol Number: PrevSVD-2015 | Start Date*: 2015-10-09 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||||||||||||||||||||||
Full Title: Preventing cognitive decline and dementia from cerebral small vessel disease | |||||||||||||||||||||||||||||||||
Medical condition: Lacunar (small vessel) ischaemic stroke | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000110-19 | Sponsor Protocol Number: P060406 | Start Date*: 2012-01-10 | |||||||||||||||||||||
Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | |||||||||||||||||||||||
Full Title: Closure of patent foramen ovale or anticoagulants versus antiplatelet therapy to prevent stroke recurrence | |||||||||||||||||||||||
Medical condition: The study compares different strategies for secondary stroke (or retinal ischaemia) prevention in patients with patent foramen ovale. The three treatment arms comprise: 1. Endovascular patent f... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005749-18 | Sponsor Protocol Number: B01-02 | Start Date*: 2013-08-29 | |||||||||||||||||||||
Sponsor Name:Athersys, Inc | |||||||||||||||||||||||
Full Title: Double-Blind, Randomized, Placebo-Controlled, Phase 2 Safety and Efficacy Trial of MultiStem® in Adults With Ischemic Stroke | |||||||||||||||||||||||
Medical condition: acute ischemic stroke | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016057-17 | Sponsor Protocol Number: 23349 | Start Date*: 2011-07-14 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gentofte Hospital | ||||||||||||||||||||||||||||||||||||||
Full Title: Behandling med nerveaktiverende medicin efter apopleksi - måling af genoptræningseffekt, patologisk træthed, muskelstyrke og knogleafkalkning | ||||||||||||||||||||||||||||||||||||||
Medical condition: Apopleksi. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002327-42 | Sponsor Protocol Number: 191622-129 | Start Date*: 2014-05-21 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: Long-term Study of BOTOX® Treatment in Adult Patients with Upper Limb Spasticity | |||||||||||||||||||||||
Medical condition: Poststroke spasticity involving the muscles of the elbow and shoulder in adult patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005612-41 | Sponsor Protocol Number: 15-15 | Start Date*: 2015-11-30 | |||||||||||||||||||||||||||||||
Sponsor Name:Meander Medical Centre | |||||||||||||||||||||||||||||||||
Full Title: Vitamin c to Improve Tissue healing by Administration of Multiple INtravenous dosages | |||||||||||||||||||||||||||||||||
Medical condition: Patients with planned revascularisation surgery on the lower extremities. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000686-23 | Sponsor Protocol Number: RAVE_v1 | Start Date*: 2017-03-29 |
Sponsor Name:Erasmus MC | ||
Full Title: The Rotterdam Antiplatelet Therapy in Vascular Patients Study | ||
Medical condition: myocardial injury in patients undergoing major vascular surgery, leading to (spontaneous) acute coronary syndrome and death through intracoronary plaque damage and subsequent thrombosis after major... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021264-14 | Sponsor Protocol Number: 10-003 | Start Date*: 2012-09-25 |
Sponsor Name:RWTH Aachen University represented by the rector, himself represented by the dean of the Medical Faculty | ||
Full Title: Vitamin K1 to slow vascular calcification in hemodialysis patients. Multicenter, multinational, randomized controlled clinical trial | ||
Medical condition: dialysis patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001631-46 | Sponsor Protocol Number: NL65876.078.18 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:Erasmus University Medical Center | |||||||||||||
Full Title: Implementation of pharmacokinetic-guided dosing of DDAVP and VWF-containing concentrates in von Willebrand disease | |||||||||||||
Medical condition: Von Willebrand disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003179-32 | Sponsor Protocol Number: ToL54304 | Start Date*: 2016-02-03 | |||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
Full Title: PREvention of Complications to Improve Outcome in elderly patients with acute Stroke. A randomised, open, phase III, clinical trial with blinded outcome assessment. | |||||||||||||||||||||||
Medical condition: Stroke (ischaemic stroke or intracerebral hemorrhage) | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) HU (Completed) GR (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002351-33 | Sponsor Protocol Number: 1299 | Start Date*: 2006-08-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ISTITUTI OSPITALIERI DI VERONA | |||||||||||||
Full Title: Evaluation of safety and efficacy of intravitreal bevacizumab for macular edema, retinal or choroidal neovascularization or neovascular glaucoma | |||||||||||||
Medical condition: Macular oedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001948-60 | Sponsor Protocol Number: DOSFEM | Start Date*: 2013-09-09 |
Sponsor Name:Sint Franciscus Gasthuis Rotterdam | ||
Full Title: Effects of high and low dose vitamin D on postprandial leukocyte activation, oxidative stress and vascular function in healthy overweight and obese females | ||
Medical condition: 'healthy volunteers' 'atherosclerosis' 'vitamin D deficiency' | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004371-19 | Sponsor Protocol Number: ARC1779-004 | Start Date*: 2007-11-20 | ||||||||||||||||
Sponsor Name:Archemix Corp. | ||||||||||||||||||
Full Title: A Phase 2 Pilot Study of the Safety, Pharmacokinetics, and Pharmacodynamics of ARC1779 Injection in Patients with von Willebrand Factor-Related Platelet Function Disorders | ||||||||||||||||||
Medical condition: von Willebrand Factor- related platelet function disorders : thrombotic thrombocytopenic purpura(TTP) in remission, acute TTP, and von Willebrand Disease Type- 2b (vWD-2b). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003391-39 | Sponsor Protocol Number: 9026 | Start Date*: 2012-10-26 | |||||||||||
Sponsor Name:University Hospital of Montpellier | |||||||||||||
Full Title: Ballon aortic valvuloplasty performed without heparin to decrease vascular and bleeding complications of the procedure | |||||||||||||
Medical condition: Aortic stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004539-30 | Sponsor Protocol Number: BAY59-7939/14373 | Start Date*: 2012-10-23 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: 30-day, single-arm study of the safety, efficacy and the pharmacokinetic and pharmacodynamic properties of oral rivaroxaban in children with various manifestations of venous thrombosis | |||||||||||||
Medical condition: venous thrombosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004675-13 | Sponsor Protocol Number: WIL-31 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Octapharma AG | |||||||||||||
Full Title: CLINICAL STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF WILATE DURING PROPHYLAXIS IN PREVIOUSLY TREATED PATIENTS WITH VON WILLEBRAND DISEASE (VWD) | |||||||||||||
Medical condition: Von Willebrand disease, type 3, type 2 (except 2N), or severe type 1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) HU (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003453-16 | Sponsor Protocol Number: SHP677-304 | Start Date*: 2019-07-31 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A PHASE 3B, PROSPECTIVE, OPEN-LABEL, UNCONTROLLED, MULTICENTER STUDY ON LONGTERM SAFETY AND EFFICACY OF rVWF IN PEDIATRIC AND ADULT SUBJECTS WITH SEVERE VON WILLEBRAND DISEASE (VWD) | |||||||||||||
Medical condition: severe von Willebrand Disease | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DE (Completed) ES (Completed) AT (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001336-62 | Sponsor Protocol Number: 2019-ASPIREAF | Start Date*: 2020-04-01 | |||||||||||||||||||||
Sponsor Name:Hamilton Health Sciences Corporation | |||||||||||||||||||||||
Full Title: Anticoagulation for Stroke Prevention In patients with Recent Episodes of perioperative Atrial Fibrillation after noncardiac surgery - The ASPIRE-AF trial | |||||||||||||||||||||||
Medical condition: Perioperative atrial fibrillation after noncardiac surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003519-23 | Sponsor Protocol Number: D513BC00001 | Start Date*: 2014-02-05 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Multinational, Randomised, Double-Blind, Placebo-Controlled Trial to Evaluate the Effect of Ticagrelor twice daily on the Incidence of Cardiovascular Death, Myocardial Infarction or Stroke in Pat... | ||||||||||||||||||
Medical condition: major cardiovascular events in type 2 diabetes mellitus patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) CZ (Completed) SK (Completed) SE (Completed) NL (Completed) DE (Completed) IT (Completed) GB (Completed) ES (Completed) NO (Completed) AT (Completed) DK (Completed) BE (Completed) FI (Completed) BG (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000709-38 | Sponsor Protocol Number: BBR | Start Date*: 2015-10-20 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: Acute Effects of Benzbromaron on the pulmonary circulation | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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