- Trials with a EudraCT protocol (77)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
77 result(s) found for: Cerebral ischemia.
Displaying page 1 of 4.
EudraCT Number: 2007-000359-33 | Sponsor Protocol Number: 0604002 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:CHU Toulouse | |||||||||||||
Full Title: PENOMBRE HYPOXIQUE ET ISCHEMIE SEMI-TARDIVE ETUDIEE EN TEP AU 18F-FLUOROMISONIDAZOLE : IMPACT SUR LA RECUPERATION FONCTIONNELLE DANS LES SUITES D’UN AVC ISCHEMIQUE AVEC DEFICIT MOTEUR. Etude de ... | |||||||||||||
Medical condition: Accident vasculaire cérébral | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000846-32 | Sponsor Protocol Number: SELEIS | Start Date*: 2014-11-06 | |||||||||||
Sponsor Name:Fundació Privada Hospital Asil de Granollers | |||||||||||||
Full Title: EFFECT OF SEROTONIN AND LEVODOPA FUNCTIONAL RECOVERY IN PATIENTS WITH CEREBRAL INFARCTION | |||||||||||||
Medical condition: Functional recovery in patients with cerebral infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000509-58 | Sponsor Protocol Number: RC31/18/0472 | Start Date*: 2019-10-08 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: Cerebral hemodynamic optimization by milrinone for the prevention of delayed cerebral ischemia in severe subarachnoid hemorrhages | |||||||||||||
Medical condition: delayed cerebral ischemia in severe subarachnoid hemorrhages | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006731-31 | Sponsor Protocol Number: tandem-1 | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:Fundació Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol | |||||||||||||
Full Title: Estudio doble ciego, aleatorizado, controlado con placebo de dosis escaladas de deferoxamina intravenosa en pacientes con ictus isquémico agudo tratado con activador tisular del plasminógeno. Doubl... | |||||||||||||
Medical condition: La deferoxamina es un neuroprotector en modelos animales de isquemia/reperfusión cerebral. Si la deferoxamina es segura y bien tolerada en pacientes con ictus agudo puede significar una nueva estra... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002784-34 | Sponsor Protocol Number: NL69665.091.19 | Start Date*: 2020-01-08 | ||||||||||||||||
Sponsor Name:Radboudumc [...] | ||||||||||||||||||
Full Title: Deferoxamine in Aneurysmal Subarachnoid Hemorrhage pilot trial | ||||||||||||||||||
Medical condition: patients with aneurysmal subarachnoid hemorrhage | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000702-19 | Sponsor Protocol Number: LITE | Start Date*: 2015-07-22 | ||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||
Full Title: Haemostatic and Fibrinolytic Analysis of Low Molecular Weight Heparin Injections versus Unfractionated Heparin Infusion as Post-CABG Thromboprophylaxis | ||||||||||||||||||
Medical condition: Deep venous thrombosis, myocardial infarction, cerebral infarction, bleeding | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2018-000790-79 | Sponsor Protocol Number: 2018-000790-79 | Start Date*: 2021-08-09 |
Sponsor Name:Academic Medical Centre Amsterdam | ||
Full Title: IMPROVING OUTCOME IN SUBARACHNOID HEMORRHAGE WITH NADROPARINE | ||
Medical condition: Patients suffering from an aneurysmal subarachnoid hemorrhage. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000241-39 | Sponsor Protocol Number: ID-054-304 | Start Date*: 2018-08-27 | ||||||||||||||||
Sponsor Name:Idorsia Pharmaceuticals Ltd | ||||||||||||||||||
Full Title: A prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group, Phase 3 study to assess the efficacy and safety of clazosentan in preventing clinical deterioration due to... | ||||||||||||||||||
Medical condition: Aneurysmal Subarachnoid Hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) DE (Completed) SE (Completed) FR (Completed) CZ (Completed) BE (Completed) DK (Completed) HU (Completed) AT (Completed) PL (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000586-33 | Sponsor Protocol Number: 19-PP-15 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Effect of molar sodium lactate infusion on cerebral hemodynamic in patients with severe subarachnoid hemorrhage: a multicenter double-blind randomized controlled study | |||||||||||||
Medical condition: Subarachnoid hemorrhage caused by rupture of cerebral aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002151-10 | Sponsor Protocol Number: NEUROPROTECTpost-CA | Start Date*: 2015-08-07 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Neuroprotective goal directed hemodynamic optimization in post-cardiac arrest patients: a randomized controlled trial (the NEUROPROTECT post-CA trial) | |||||||||||||
Medical condition: post-cardiac arrest patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001702-30 | Sponsor Protocol Number: 200175 | Start Date*: 2022-02-08 |
Sponsor Name:APHP | ||
Full Title: « Use of Levosimendan as treatment of aneurysmal SubArachnoid Hemorrhage » | ||
Medical condition: subarachnoid hemorrhages of aneurysmal origin (HSAa) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000996-98 | Sponsor Protocol Number: CSL112_3001 | Start Date*: 2018-09-05 | |||||||||||
Sponsor Name:CSL Behring LLC | |||||||||||||
Full Title: A Phase 3, Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Efficacy and Safety of CSL112 in Subjects with Acute Coronary Syndrome | |||||||||||||
Medical condition: Acute Coronary Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Temporarily Halted) LV (Completed) SE (Completed) PT (Completed) FI (Completed) BE (Completed) LT (Completed) DK (Completed) EE (Completed) DE (Completed) AT (Completed) CZ (Completed) NO (Completed) HU (Completed) FR (Completed) NL (Completed) ES (Restarted) SK (Completed) BG (Completed) GR (Completed) HR (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005254-24 | Sponsor Protocol Number: HA009 | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:Nuvelo, Inc | |||||||||||||
Full Title: PHASE 2, MULTICENTER, OPEN-LABEL, TWO-STAGE STUDY TO EVALUATE THE SAFETY AND EFFICACY OF INTRA-ARTERIAL CATHETER-DIRECTED ALFIMEPRASE FOR RESTORATION OF NEUROLOGIC FUNCTION AND RAPID OPENING OF ART... | |||||||||||||
Medical condition: Acute Ischemic Stroke (AIS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006749-42 | Sponsor Protocol Number: 31350 | Start Date*: 2009-01-09 | ||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||
Full Title: Safety and efficacy of clopidogrel when added to aspirin and dipyridamole in high risk patients with recent ischaemic stroke or TIA: a randomised controlled trial | ||||||||||||||||||
Medical condition: Ischaemic stroke and TIA (transient ischaemic attack) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000343-26 | Sponsor Protocol Number: ULTRA12 | Start Date*: 2012-09-06 |
Sponsor Name:Academic Medical Center, Neurosurgery | ||
Full Title: Ultra-early tranexamic acid after subarachnoid hemorrhage. A prospective, randomized, multicenter study. | ||
Medical condition: subarachnoid hemorrhage | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003176-38 | Sponsor Protocol Number: 135.312 | Start Date*: 2006-05-22 |
Sponsor Name:Boehringer Ingelheim Pharma Ges mbH | ||
Full Title: A placebo controlled trial of alteplase (rt-PA) in acute ischemic hemispheric stroke where thrombolysis is initiated between 3 and 4 hours 30 minutes after stroke onset | ||
Medical condition: Ischemic stroke 3 and 4 hours 30 minutes before treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) SK (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-006177-88 | Sponsor Protocol Number: FARM65KNKY | Start Date*: 2008-01-24 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: A randomized controlled trial of alteplase (rt-PA) vs standard treatment in acute ischemic hemispheric stroke in patients aged more than 80 years where thrombolysis is initiated within 3 hours afte... | |||||||||||||
Medical condition: acute ischemic stroke | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021360-15 | Sponsor Protocol Number: IG0905 | Start Date*: 2010-12-20 | |||||||||||
Sponsor Name:Instituto Grifols S.A. | |||||||||||||
Full Title: "EFECTOS DEL RECAMBIO PLASMÁTICO SOBRE LA CAPACIDAD FUNCIONAL DE LA ALBÚMINA SÉRICA, LA DISFUNCIÓN CIRCULATORIA, LA FUNCION RENAL Y CEREBRAL EN PACIENTES CIRRÓTICOS CON ACUTE-ON-CHRONIC LIVER FAIL... | |||||||||||||
Medical condition: Pacientes cirróticos con "Acute on chronic liver failure" | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001300-30 | Sponsor Protocol Number: 2017_CERVPLEX_1.1 | Start Date*: 2017-10-03 |
Sponsor Name:UK für Anästhesieologie, Gemeinn. Sbg. Landeskliniken BetriebsgesmbH | ||
Full Title: Comparison of deep, intermediate and superficial cervical plexus block for carotid endarterectomies concerning paresis of the phrenic nerve, lung function and tissue distribution: a prospective, ra... | ||
Medical condition: deep, intermediate or superficial cervical plexus block for carotid endarterectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
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