- Trials with a EudraCT protocol (159)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
159 result(s) found for: Acute Ischaemic Stroke AND Ischaemic Stroke.
Displaying page 4 of 8.
EudraCT Number: 2008-005041-33 | Sponsor Protocol Number: MAG111539 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Single-Blind Study of the Safety, Pharmacokinetics and Pharmacodynamics of Escalating Repeat Doses of GSK249320 in Patients With Stroke. | |||||||||||||
Medical condition: Patients with Stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005868-26 | Sponsor Protocol Number: stars07 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:Neurovascular Research Group-IRVH | |||||||||||||
Full Title: Estrategias para mejorar la eficacia y seguridad del tratamiento con Simvastatina en la Fase Aguda del Ictus Isquémico: STARS trial. Improving Safety and Efficacy of Simvastatin Treatment for the... | |||||||||||||
Medical condition: Stroke. Ischemic Stroke. Ictus. Ictus isquémico. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000123-33 | Sponsor Protocol Number: RH EPOA-REHAB | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
Full Title: Evaluation of the feasibility of modulating and measuring endogenous neurogenesis with erythropoietin (rhEPOα) to expedite recovery after stroke | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003783-27 | Sponsor Protocol Number: PN06-CLD-01001 | Start Date*: 2006-01-26 | |||||||||||
Sponsor Name:PAION Deutschland GmbH | |||||||||||||
Full Title: TOLERABILITY OF ENECADIN (INN) IN ACUTE ISCHEMIC STROKE TRIAL - TEST- PHASE IIA : A multicentre, double-blind, randomised, placebo-controlled, dose-escalating parallel- group study to investigate t... | |||||||||||||
Medical condition: acute ischemic stoke Based on the results of preclinical studies, enecadin is expected to play an important role in the treatment of acute ischemic stroke and to ameliorate the outcome and prognos... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003551-18 | Sponsor Protocol Number: AMASCIS-01/2011 | Start Date*: 2012-07-23 | |||||||||||
Sponsor Name:FIBHULP | |||||||||||||
Full Title: Reparative Therapy In Acute Ischemic Stroke With Alogeneic Mesenchymal Stem Cells From Adipose Tissue. Safety Assessment. A Randomised, Double Blind Placebo? Controlled Single Center Pilot Clinical... | |||||||||||||
Medical condition: acute ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005345-11 | Sponsor Protocol Number: RA2364 | Start Date*: 2007-08-08 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: ‘Stem cell Trial of recovery EnhanceMent after Stroke 2’ (STEMS2) pilot randomised placebo-controlled trial of granulocyte-colony stimulating factor in mobilising bone marrow stem cells in sub-acu... | |||||||||||||
Medical condition: Ischaemic and Haemorrhagic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001005-16 | Sponsor Protocol Number: CL2-44819-004 | Start Date*: 2016-09-21 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Randomized Efficacy and Safety Trial with Oral S 44819 after Recent ischemic cerebral Event. International, multi-centre, randomized, double-blind placebo-controlled phase II study. | |||||||||||||
Medical condition: Post stroke recovery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) SE (Completed) DE (Completed) BE (Completed) NL (Completed) ES (Completed) PL (Completed) CZ (Completed) SI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003479-11 | Sponsor Protocol Number: 06/Q2604/75 | Start Date*: 2007-05-22 |
Sponsor Name:North Staffordshire Combined Healthcare Trust | ||
Full Title: The Stroke Oxygen Study. A randomised controlled study of the benefits and risks of routine oxygen treatment after acute stroke | ||
Medical condition: Acute Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002747-29 | Sponsor Protocol Number: BIA-2093-213 | Start Date*: 2019-04-24 | |||||||||||
Sponsor Name:Bial - Portela & Ca, S.A. | |||||||||||||
Full Title: Prevention of epilepsy in stroke patients at high risk of developing unprovoked seizures: anti-epileptogenic effects of eslicarbazepine acetate | |||||||||||||
Medical condition: Adult patients at high-risk to develop post-stroke epilepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) GB (GB - no longer in EU/EEA) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001989-42 | Sponsor Protocol Number: TEA-Stroke | Start Date*: 2013-08-02 | |||||||||||
Sponsor Name:Boris Modrau | |||||||||||||
Full Title: Theophylline Effect in Acute Ischemic Stroke Trial | |||||||||||||
Medical condition: Acute ischemic stroke patients eligible for standard intravenous recombinant tissue plasminogen activator (rtPA) thrombolytic therapy with magnet resonance imaging (MRI)-proved infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002456-88 | Sponsor Protocol Number: Stroke34 | Start Date*: 2023-02-28 | |||||||||||
Sponsor Name:CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA, E.P.E | |||||||||||||
Full Title: STROKE34: randomized controlled phase IIa trial of intra-arterial CD34+ cells in acute ischemic stroke. | |||||||||||||
Medical condition: Acute ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024048-14 | Sponsor Protocol Number: CRO1793 | Start Date*: 2011-12-22 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A randomised-controlled trial of donepezil for motor recovery in acute stroke | ||||||||||||||||||
Medical condition: Acute stroke (ischemic and hemorrhagic strokes, starting within 4 days of onset) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006130-16 | Sponsor Protocol Number: EFFECTS2012 | Start Date*: 2014-08-08 |
Sponsor Name:Karolinska Institutet | ||
Full Title: ESTABLISHING THE EFFECT(S) AND SAFETY OF FLUOXETINE INITIATED IN THE ACUTE PHASE OF STROKE | ||
Medical condition: Cerebrovascular diseases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004748-27 | Sponsor Protocol Number: EPIDAURUS-2020 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:LMU University Hospital Munich | |||||||||||||
Full Title: Escalated single platelet inhibition for one month plus direct oral anticoagulation in patients with atrial fibrillation and acute coronary syndrome undergoing percutaneous coronary intervention | |||||||||||||
Medical condition: Patients with atrial fibrillation and ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) (biomarker -positive acute coronary syndrome) und... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000622-40 | Sponsor Protocol Number: 12402A | Start Date*: 2009-01-21 | |||||||||||
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: NL (Prematurely Ended) HU (Completed) AT (Completed) DE (Prematurely Ended) FR (Completed) ES (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005491-40 | Sponsor Protocol Number: MRX-06-101-CP-01-01 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:ImaRx Therapeutics, Inc | |||||||||||||
Full Title: A Phase 1-2, Randomized, Placebo-Controlled, Single-Blind, Dose Escalation Study to Evaluate the Safety, Tolerability, and Activity of Ascending Single Doses of MRX-801 with Continuous Ultrasound A... | |||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003090-95 | Sponsor Protocol Number: NOR-TEST2 | Start Date*: 2019-02-12 |
Sponsor Name:Helse Bergen HF | ||
Full Title: The Norwegian Tenecteplase Stroke Trial 2 ( NOR-TEST 2 ) Tenecteplase in Acute Stroke 2 | ||
Medical condition: Ischeamic stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017315-15 | Sponsor Protocol Number: NTR1804 | Start Date*: 2010-06-10 | |||||||||||
Sponsor Name:Erasmus MC Rotterdam | |||||||||||||
Full Title: Multi Center Clinical trial of endovascular treatment of acute ischemic stroke in the Netherlands. | |||||||||||||
Medical condition: Acute ischemic brain infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007197-31 | Sponsor Protocol Number: 3001088 | Start Date*: 2008-04-22 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
Full Title: EFFECTS OF ORAL LEVOSIMENDAN ON AMBULATORY ELECTROCARDIOGRAPHIC VARIABLES AND CEREBROVASCULAR REACTIVITY IN PATIENTS WITH RECENT STROKE OR TIA. A RANDOMISED, DOUBLE BLIND, PLACEBO-CONTROLLED, DOSE ... | |||||||||||||
Medical condition: Stroke or TIA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Prematurely Ended) HU (Completed) DE (Completed) | |||||||||||||
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 |
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