- Trials with a EudraCT protocol (310)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
310 result(s) found for: Acute Ischemic Stroke.
Displaying page 2 of 16.
EudraCT Number: 2008-006444-19 | Sponsor Protocol Number: AX200-101 | Start Date*: 2009-05-12 | |||||||||||
Sponsor Name:SYGNIS Bioscience GmbH & Co. KG | |||||||||||||
Full Title: AXIS 2: AX200 for the treatment of ischemic stroke A multinational, multicenter, randomized, doubleblind, placebo-controlled, phase II trial | |||||||||||||
Medical condition: ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) CZ (Completed) ES (Completed) SE (Prematurely Ended) PL (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001680-69 | Sponsor Protocol Number: B01-04 | Start Date*: 2021-05-17 | |||||||||||
Sponsor Name:Athersys, Inc. | |||||||||||||
Full Title: MultiStem® Administration for Stroke Treatment and Enhanced Recovery Study (MASTERS-2) | |||||||||||||
Medical condition: Acute ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008298-77 | Sponsor Protocol Number: CV185-068 | Start Date*: 2009-04-14 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Apixaban for Prevention of Acute Ischemic Events - 2 A Phase 3, Randomized, Double-Blind, Evaluation of the Safety and Efficacy of Apixaban In Subjects with a Recent Acute Coronary Syndrome | |||||||||||||
Medical condition: Subjects with a recent acute coronary syndrome (ACS) and at least 2 additional risk factors for recurrent ischemic events. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) AT (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) NO (Completed) ES (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) DK (Completed) CZ (Prematurely Ended) BE (Completed) HU (Prematurely Ended) DE (Completed) BG (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004512-32 | Sponsor Protocol Number: FARM6LN3KS | Start Date*: 2007-09-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA' GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: SYNTHESIS: A RANDOMIZED CONTROLLED TRIAL ON INTRA-ARTERIAL VERSUS INTRAVENOUS THROMBOLYSIS IN ACUTE ISCHEMIC STROKE | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000238-36 | Sponsor Protocol Number: IST-399 | Start Date*: 1999-10-05 | |||||||||||
Sponsor Name:The University of Edinburgh & Lothian Health Board | |||||||||||||
Full Title: Third International Stroke Trial (IST-3) of thrombolysis for acute ischaemic stroke | |||||||||||||
Medical condition: Acute ischaemic stroke refers to strokes caused by thrombosis or embolism and accounts for 85% of all strokes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000075-85 | Sponsor Protocol Number: I-StrokeII2016 | Start Date*: 2018-06-19 | ||||||||||||||||
Sponsor Name:Karolinska Institutet | ||||||||||||||||||
Full Title: A phase 3, randomised, double-blind, placebo-controlled, parallel-arm efficacy trial of Imatinib in acute ischaemic stroke | ||||||||||||||||||
Medical condition: Patients with acute ischaemic stroke and an imaging scan excluding any intracranial haemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000313-20 | Sponsor Protocol Number: 1208094 | Start Date*: 2013-06-14 | |||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||
Full Title: Evaluation of the biological response to clopidogrel in patients with ischemic stroke: role of platelet alpha2-adrenergic receptors | |||||||||||||
Medical condition: Ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006829-13 | Sponsor Protocol Number: 2005B118 | Start Date*: 2008-02-19 |
Sponsor Name:Netherlands Heart Foundation | ||
Full Title: Antiplatelet therapy in combination with Recombinant t-PA Thrombolysis in Ischemic Stroke | ||
Medical condition: Patients with ischemic stroke More specific patients with ischemic stroke treated with rt-PA thrombolysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003959-22 | Sponsor Protocol Number: CV006-004 | Start Date*: 2016-09-06 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 2, Placebo Controlled, Randomized, Double-Blind, Parallel-Arm Study to Evaluate Efficacy and Safety of BMS-986141 For the Prevention of Recurrent Brain Infarction in Subjects receiving acet... | ||||||||||||||||||
Medical condition: Recurrent Brain Infarction in Subjects receiving acetylsalicyl acid (ASA) following Acute Ischemic Stroke or Transient Ischemic Attack | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004681-16 | Sponsor Protocol Number: NTI-ASP-0502 | Start Date*: 2006-04-24 |
Sponsor Name:Neurobiological Technologies Inc | ||
Full Title: ASP I (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment within 6 Hour... | ||
Medical condition: Acute Ischemic Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005029-19 | Sponsor Protocol Number: CV010031 | Start Date*: 2020-06-09 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Global, Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of BMS-986177, an Oral Factor XIa Inhibitor, for the Prevention of New Ischemic Stroke or New Covert Brain Infarc... | ||||||||||||||||||
Medical condition: Ischemic Stroke or Transient Ischemic Attack (TIA) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Ongoing) SE (Completed) HU (Completed) NO (Completed) FI (Completed) BE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) DK (Completed) GR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-006067-31 | Sponsor Protocol Number: NTI-ASP-0503 | Start Date*: 2008-04-04 |
Sponsor Name:Neurobiological Technologies Inc | ||
Full Title: ASP II (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment within 6 Hou... | ||
Medical condition: Acute Ischemic Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) AT (Prematurely Ended) SK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001982-36 | Sponsor Protocol Number: AcT_CZE | Start Date*: 2020-08-19 | ||||||||||||||||
Sponsor Name:Fakultní nemocnice u sv. Anny | ||||||||||||||||||
Full Title: Alteplase compared to tenecteplase in patients with acute ischemic stroke: Registry-based pragmatic randomized controlled trial | ||||||||||||||||||
Medical condition: Acute ischemic stroke | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002760-41 | Sponsor Protocol Number: CL2-RTCCAR-001 | Start Date*: 2017-09-18 | |||||||||||
Sponsor Name:institute de Recherches Internacionales Servier (promotor internacional) | |||||||||||||
Full Title: Assessment of Active Thrombin-Activatable Fibrinolysis Inhibitor (TAFIa) plasma kinetics in Patients at acute stage of Ischemic Stroke: Prospective, Multicentre, Open, Non-randomised, Biomarker Study | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004898-41 | Sponsor Protocol Number: NBK241/1/2020 | Start Date*: 2021-03-31 | |||||||||||
Sponsor Name:MEDICAL UNIVERSITY OF GDAŃSK | |||||||||||||
Full Title: A multicentre, parallel group, randomised, double blind, placebo-controlled, phase II study evaluating the efficacy and safety of reperfusion thrombolytic therapy with intravenous recombinant tissu... | |||||||||||||
Medical condition: Acute ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003895-38 | Sponsor Protocol Number: D5134C00001 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, double-blind, multinational study to prevent major vascular events with Ticagrelor compared to Aspirin(ASA) in patients with acute ischaemic stroke or Transient Ischemic Attack (TIA).... | |||||||||||||
Medical condition: ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) BE (Completed) SE (Completed) DE (Completed) IT (Completed) ES (Completed) BG (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002864-33 | Sponsor Protocol Number: NTA0903 | Start Date*: 2014-12-16 | ||||||||||||||||
Sponsor Name:The Florey Institute of Neuroscience and Mental Health | ||||||||||||||||||
Full Title: EXTEND (International): Extending the time for Thrombolysis in Emergency Neurological Deficits (International) | ||||||||||||||||||
Medical condition: Ischaemic stroke | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001514-15 | Sponsor Protocol Number: 101SK201 | Start Date*: 2013-11-26 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischem... | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005980-26 | Sponsor Protocol Number: MAAS | Start Date*: 2012-07-04 | ||||||||||||||||||||||||||
Sponsor Name: | ||||||||||||||||||||||||||||
Full Title: Metformin and sitagliptin in patients with impaired glucose tolerance and a recent TIA or minor ischemic stroke - a multicenter, randomized, open-label phase II trial | ||||||||||||||||||||||||||||
Medical condition: Stroke Transient ischemic attack Impaired glucose tolerance | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024541-67 | Sponsor Protocol Number: 1 | Start Date*: 2011-11-10 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde R&D Office [...] | |||||||||||||
Full Title: Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis – pilot phase | |||||||||||||
Medical condition: Acute Ischaemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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