- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Intracerebral Haemorrhagic Stroke.
Displaying page 1 of 2.
EudraCT Number: 2020-004746-10 | Sponsor Protocol Number: NTA1702 | Start Date*: 2021-01-27 | |||||||||||||||||||||||||||||||
Sponsor Name:The Florey Institute of Neuroscience and Mental Health | |||||||||||||||||||||||||||||||||
Full Title: STOP-MSU – Stopping haemorrhage with Tranexamic acid for hyperacute Onset Presentation including Mobile Stroke Units | |||||||||||||||||||||||||||||||||
Medical condition: Intracerebral Haemorrhage | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-004108-37 | Sponsor Protocol Number: 12101 | Start Date*: 2012-11-23 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Tranexamic acid for hyperacute primary IntraCerebral Haemorrhage TICH-2 | |||||||||||||
Medical condition: Primary Intracerebral Haemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) ES (Completed) HU (Completed) DK (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006206-24 | Sponsor Protocol Number: Aivoverenvuotopotilaan tromboosipro | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:Hillbom Matti OYS/neurologian klinikka | |||||||||||||
Full Title: A blind randomized trial to compare the efficacy of intermittent pneumatic compression (IPC) with and without early anticoagulant treatment for prevention of venous thromboembolism (VTE) in patient... | |||||||||||||
Medical condition: Spontaani aivoverenvuoto | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005738-23 | Sponsor Protocol Number: CBAF312X2207 | Start Date*: 2018-06-15 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A phase II, patient and investigator-blinded, randomized, placebo-controlled study to evaluate efficacy, safety and tolerability of BAF312 in patients with stroke due to intracerebral hemorrhage (ICH) | |||||||||||||
Medical condition: Intracerebral Hemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000602-73 | Sponsor Protocol Number: LEX-206 | Start Date*: 2008-02-07 | |||||||||||||||||||||
Sponsor Name:OCTAPHARMA AG | |||||||||||||||||||||||
Full Title: Efficacy and Safety of two doses regimens of Octaplex in patients with cerebral haemorrhage related to oral anticoagulant therapy: A phase IV, prospective, randomised, open-label study. | |||||||||||||||||||||||
Medical condition: Traitement des saignements et prophylaxie péri-opératoire des accidents hémorragiques en cas de déficit acquis en facteurs de coagulation du complexe prothrombique, notamment induit par les anti-vi... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-004202-24 | Sponsor Protocol Number: F7ICH-1641 | Start Date*: 2005-04-29 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Randomised, Double-Blind, Placebo Controlled, Multi-Centre, Parallel Groups Confirmatory Efficacy and Safety Trial of Activated Recombinant Factor VII (NovoSeven®/Niastase®) in Acute Intracerebral ... | |||||||||||||
Medical condition: Acute Intracerebral Haemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) NO (Completed) DK (Completed) IT (Completed) BE (Completed) AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022009-16 | Sponsor Protocol Number: 1.0 | Start Date*: 2010-11-01 |
Sponsor Name:University of Nottingham | ||
Full Title: A randomised controlled trial of Tranexamic acid in Intracerebral Haemorrhage (TICH) | ||
Medical condition: Primary intracerebral haemorrhage | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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: 2008-005653-37 | Sponsor Protocol Number: ICH-VKA | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Universityhospital of Heidelberg | |||||||||||||
Full Title: Multicenter, prospective randomized trial on the use of prothrombin complex and fresh frozen plasma in patients with intracerebral hemorrhage related to vitamin K antagonists (VKA) | |||||||||||||
Medical condition: Intracerebral hemorrhage (ICH) in patients related to vitamin K antagonists | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Suspended by CA) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004121-16 | Sponsor Protocol Number: AC16141 | Start Date*: 2017-09-11 | |||||||||||
Sponsor Name:University of Edinburgh | |||||||||||||
Full Title: Start or STop Anticoagulants Randomised Trial (SoSTART) after spontaneous intracranial haemorrhage | |||||||||||||
Medical condition: Spontaneous Intracranial Haemorrhage (ICH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000230-53 | Sponsor Protocol Number: TMC-CLV-07-02 | Start Date*: 2008-05-15 | ||||||||||||||||
Sponsor Name:The Medicines Company | ||||||||||||||||||
Full Title: The evaluation of patients with acute hypertension and intracerebral hemorrhage with intravenous clevidipine treatment | ||||||||||||||||||
Medical condition: Acute hypertension in patients who present with intracerebral hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006006-22 | Sponsor Protocol Number: ICH01 | Start Date*: 2009-01-14 | |||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Trust [...] | |||||||||||||
Full Title: Minimally Invasive Surgery plus rt-PA for ICH Evacuation | |||||||||||||
Medical condition: intracerebral hemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002433-15 | Sponsor Protocol Number: RS200511 | Start Date*: 2021-02-15 | ||||||||||||||||||||||||||
Sponsor Name:Region Skåne | ||||||||||||||||||||||||||||
Full Title: Positron emission tomography (PET) of patients with brain injury and athletes with concussion symptoms - Descriptive study of the tau tracer 18F-RO6958948 | ||||||||||||||||||||||||||||
Medical condition: Traumatic brain injury (TBI), cerebral haemorrhage (ICH), subarachnoid haemorrhage (SAH) and cerebral commotio. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004521-17 | Sponsor Protocol Number: BIT-001 | Start Date*: 2018-02-19 | |||||||||||
Sponsor Name:BIT Pharma GmbH | |||||||||||||
Full Title: A Phase IIa: single ascending dose safety, tolerability and pharmacokinetic study of NicaPlant® in aneurysmal subarachnoid haemorrhage patients undergoing aneurysm clipping | |||||||||||||
Medical condition: Aneurysmal subarachnoid haemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003190-26 | Sponsor Protocol Number: RESTART13 | Start Date*: 2013-01-14 | |||||||||||
Sponsor Name:ACCORD (Academic and Clinical Central Office for Research & Development) [...] | |||||||||||||
Full Title: REstart or STop Antithrombotics Randomised Trial (RESTART) | |||||||||||||
Medical condition: Spontaneous Intracerebral Haemorrhage (ICH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002176-41 | Sponsor Protocol Number: 17HH4268 | Start Date*: 2019-09-03 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Imperial College of Science Technology and Medicine | ||||||||||||||||||||||||||||||||||||||
Full Title: PREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation (PRESTIGE-AF) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Ischaemic stroke prevention in patients with atrial fibrillation and previous intracerebral haemorrhage | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) AT (Completed) FR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000112-33 | Sponsor Protocol Number: NL47761.041.14 | Start Date*: 2014-09-01 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Apixaban versus antiplatelet drugs or no antithrombotic drugs after anticoagulation-associated intracerebral haemorrhage in patients with atrial fibrillation. A randomised phase II clinical trial. | ||
Medical condition: The prevention of ischaemic stroke in patients with atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003724-23 | Sponsor Protocol Number: GI-AU-NMH-2016-01 | Start Date*: 2017-12-28 | |||||||||||
Sponsor Name:The George Institute for Global Health, University of New South Wales | |||||||||||||
Full Title: Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trial | |||||||||||||
Medical condition: Patients with a history of acute stroke due to Intracranial Haemorrhage with mild to moderately high blood pressure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001904-12 | Sponsor Protocol Number: 18040 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Desmopressin for reversal of Antiplatelet drugs in Stroke due to Haemorrhage (DASH) | |||||||||||||
Medical condition: Intracerebral haemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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 |
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