- Trials with a EudraCT protocol (499)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
499 result(s) found for: Ischemic stroke.
Displaying page 1 of 25.
EudraCT Number: 2022-001067-27 | Sponsor Protocol Number: 20604 | Start Date*: 2022-11-10 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A multicenter, international, randomized, placebo controlled, double-blind, parallel group and event driven Phase 3 study of the oral FXIa inhibitor asundexian (BAY 2433334) for the prevention of i... | |||||||||||||||||||||||
Medical condition: Prevention of ischemic stroke in patients post acute non-cardioembolic ischemic stroke or high-risk transient ischemic attack | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) NO (Trial now transitioned) LT (Trial now transitioned) HU (Trial now transitioned) ES (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) LV (Trial now transitioned) PT (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005541-12 | Sponsor Protocol Number: 2011-397 | Start Date*: 2012-02-27 | |||||||||||
Sponsor Name:Grethe Andersen | |||||||||||||
Full Title: Efficacy of escitalopram treatment in acute stroke and the role of SERT genotype in stroke | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002360-30 | Sponsor Protocol Number: NA-1-009 | Start Date*: 2021-01-05 | |||||||||||||||||||||||||||||||
Sponsor Name:NoNO Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Multicentre, Randomized, Double-blinded, Placebo-controlled, Parallel Group, Single-dose Design to Determine the Efficacy and Safety of Nerinetide in Participants with Acute Ischemic Stroke Under... | |||||||||||||||||||||||||||||||||
Medical condition: Acute ischemic stroke (AIS) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) NO (Prematurely Ended) IT (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002253-30 | Sponsor Protocol Number: 2011/397 | Start Date*: 2013-09-11 | |||||||||||
Sponsor Name:Neurological Department, Aarhus University Hospital | |||||||||||||
Full Title: Efficacy of citalopram treatment in acute stroke | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003123-22 | Sponsor Protocol Number: JCS-CBG-2014-01 | Start Date*: 2015-01-02 |
Sponsor Name:José Castillo Sanchez | ||
Full Title: "Randomized clinical trial with two parallel groups, double-blind, placebo-controlled trial to investigate whether administration of CBG000592 (riboflavin/vitamin B2) in patients with acute ischemi... | ||
Medical condition: Acute ischemic stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002404-41 | Sponsor Protocol Number: MOSES | Start Date*: 2022-08-26 |
Sponsor Name:PD Dr. med. Mira Katan | ||
Full Title: Midregional proatrial natriuretic peptide to guide secondary stroke prevention: The MOSES-study | ||
Medical condition: Patients with ischemic stroke and elevated midregional proatrial natriuretic peptide (MRproANP) levels without known atrial fibrillation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001355-31 | Sponsor Protocol Number: PROOF | Start Date*: 2022-07-15 | ||||||||||||||||
Sponsor Name:Eberhard-Karls University Tübingen represented by University Hospital Tübingen and its Commercial Director | ||||||||||||||||||
Full Title: Penumbral Rescue by Normobaric O=O Administration in Patients with Ischemic Stroke and Target Mismatch ProFile: A Phase II Proof-of-Concept Trial | ||||||||||||||||||
Medical condition: Acute ischemic stroke | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) CZ (Completed) FI (Completed) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003431-33 | Sponsor Protocol Number: 19766 | Start Date*: 2020-03-05 | ||||||||||||||||
Sponsor Name:Bayer AG | ||||||||||||||||||
Full Title: Multicenter, randomized, placebo-controlled, double-blind, parallel group, dose-finding Phase 2 study to evaluate efficacy and safety of BAY 2433334 in patients following an acute non-cardioembolic... | ||||||||||||||||||
Medical condition: Non-cardioembolic ischemic stroke | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) GB (GB - no longer in EU/EEA) ES (Completed) PT (Completed) FI (Completed) DE (Completed) NL (Completed) AT (Completed) FR (Completed) HU (Completed) DK (Completed) BE (Completed) BG (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002079-28 | Sponsor Protocol Number: 0724-018 | Start Date*: 2008-10-30 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase IIa Randomized, Double-Blind, Parallel-Groups, Placebo-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0724 Intravenous Infusion on the Amelioration of Neurological Damage ... | |||||||||||||
Medical condition: Middle cerebral artery ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003548-38 | Sponsor Protocol Number: 2015-1CR | Start Date*: 2015-09-29 | |||||||||||
Sponsor Name:Roskilde Hospital | |||||||||||||
Full Title: CLOpidogrel response and CYP2C19 Genotype in Ischemic Stroke patients | |||||||||||||
Medical condition: Ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007031-41 | Sponsor Protocol Number: BIAS1.0 | Start Date*: 2009-09-17 | ||||||||||||||||||||||||||
Sponsor Name:Center for Stroke Research Berlin - Charité Universitätsmedizin Berlin | ||||||||||||||||||||||||||||
Full Title: Beta-Blocker in Acute Ischemic Stroke – a prospective, randomized, double-blinded, placebo-controlled safety and efficacy trial of early treatment | ||||||||||||||||||||||||||||
Medical condition: Acute ischemic stroke in the A. cerebri media territory | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012025-11 | Sponsor Protocol Number: 01373 | Start Date*: 2010-01-26 | |||||||||||
Sponsor Name:D-Pharm Ltd. | |||||||||||||
Full Title: A double blind, randomized, placebo-controlled, parallel group, multicenter Phase 3 pivotal study to assess the safety and efficacy of 1mg/kg/day intravenous DP-b99 over 4 consecutive days versus... | |||||||||||||
Medical condition: Acute Ischemic Stroke Stroke is the most common neurologic disorder and is the third leading cause of death in developed countries, after myocardial infarction and cancer. Stroke is the second l... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) PT (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) FR (Completed) AT (Prematurely Ended) SK (Completed) IT (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004783-11 | Sponsor Protocol Number: 101SK202 | Start Date*: 2016-04-26 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group, Dose-Ranging Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) in Acute Ischemic Stroke | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005317-37 | Sponsor Protocol Number: THR-2010-01 | Start Date*: 2012-06-14 | |||||||||||
Sponsor Name:Thrombotech Ltd. | |||||||||||||
Full Title: Double blind, placebo controlled, escalating single-dose, pilot study to assess the safety of THR-18 when administered to patients suffering acute ischemic stroke and treated with tPA | |||||||||||||
Medical condition: Acute isquemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001729-11 | Sponsor Protocol Number: CR040301 | Start Date*: 2005-02-18 | |||||||||||
Sponsor Name:EBEWE Pharma Ges.m.b.H Nfg.KG | |||||||||||||
Full Title: A prospective, randomised, placebo controlled, double blind trial about safety and efficacy of combined treatment with Alteplase (rt-PA) and Cerebrolysin in acute ischemic hemispheric stroke | |||||||||||||
Medical condition: Clinical diagnosis of ischemic stroke causing a measurable neurological deficit defined as impairment of language, motor function, cognition and/or gaze, vision or neglect. Ischemic stroke is defin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) CZ (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005906-32 | Sponsor Protocol Number: WAKE-UP | Start Date*: 2012-09-24 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Efficacy and safety of MRI-based thrombolysis in wake-up stroke: a randomised, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: Patients with acute ischemic stroke proven by MRI and unknown time from symptom onset which otherwise fulfil the approval criteria for intravenous thrombolysis in acute stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) GB (Completed) DK (Completed) ES (Completed) NL (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005539-14 | Sponsor Protocol Number: 12649A | Start Date*: 2008-11-25 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: A randomised, double-blind, parallel-group, placebo-controlled phase III study to evaluate the efficacy and safety of desmoteplase in subjects with acute ischemic stroke. | |||||||||||||
Medical condition: Acute ischemic stroke within 3 - 9 hours after the onset of symptoms. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Prematurely Ended) FI (Prematurely Ended) IE (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) EE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004840-60 | Sponsor Protocol Number: ME1-2 | Start Date*: 2008-08-21 | |||||||||||
Sponsor Name:M's Science Corporation | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Ascending Dose, Phase IIa Study of Safety and Motor Function Restoration in Subjects Treated with SA4503 following Acute Ischemic Stroke | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003349-97 | Sponsor Protocol Number: flu2008 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:Roessingh Research&Development | |||||||||||||
Full Title: Influence of a single dose of fluoxetine on brain activity during movement observation and execution, muscle activity and motor function in chronic stroke patients | |||||||||||||
Medical condition: The objective of this study is to examine the effect of a single dose of fluoxetine and of movement observation on cortical activity in chronic stroke patients (>6 months after stroke). As secondar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002147-91 | Sponsor Protocol Number: CV185-030 | Start Date*: 2007-05-14 | ||||||||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Active (Warfarin) Controlled, Randomized, Double-Blind, Parallel Arm Study to Evaluate Efficacy and Safety of Apixaban in Preventing Stroke and Systemic Embolism in Subjects with Nonvalv... | ||||||||||||||||||
Medical condition: ARRHYTHMIA; THROMBOSIS | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) NO (Completed) BE (Completed) FI (Completed) ES (Completed) DK (Completed) HU (Completed) AT (Completed) CZ (Completed) FR (Completed) DE (Completed) IT (Completed) NL (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
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