- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Cerebral vasospasm.
Displaying page 1 of 2.
EudraCT Number: 2015-002721-18 | Sponsor Protocol Number: AC-054-203 | Start Date*: 2016-02-17 | ||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||
Full Title: A prospective, multi-center, open-label, single-arm, Phase 2 study to assess the efficacy and safety of clazosentan in reversing angiographically-confirmed cerebral vasospasm in adult subjects with... | ||||||||||||||||||
Medical condition: Aneurysmal subarachnoid hemorrhage (aSAH); cerebral vasospasm | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002584-27 | Sponsor Protocol Number: AC-054-301 | Start Date*: 2007-11-07 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group study to assess the efficacy and safety of clazosentan in reducing vasospasm-related morbidity and all-caus... | |||||||||||||
Medical condition: Indication: Aneurysmal subarachnoid hemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) FI (Completed) SE (Completed) DE (Completed) AT (Completed) DK (Completed) ES (Completed) CZ (Completed) IT (Completed) SI (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023878-40 | Sponsor Protocol Number: 2.3 | Start Date*: 2011-12-22 |
Sponsor Name:Medical University Vienna | ||
Full Title: Influence of intra-arterial cerebral Papaverine Hydrochloride on cerebral glucose, lactate, pyruvate, glycerol, and glutamate concentrations, cerebral oxygenation, angiographic vasospasm, delayed s... | ||
Medical condition: To demonstrate the influence of intra-arterial cerebral Papaverine Hydrochloride on cerebral glucose, lactate, pyruvate, glycerol, and glutamate concentrations and cerebral oxygenation in patients ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002453-31 | Sponsor Protocol Number: AC-054-201 | Start Date*: 2005-02-15 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: A Phase IIb, multi-center, international, double-blind, randomized, placebo-controlled, parallel-group, dose-finding study for the prevention of cerebral vasospasm after aneurysmal subarachnoid hem... | ||
Medical condition: Prevention of ischaemic complications related to vasospasm in patients with aneurysmal subarachnoid haemorrhage | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Completed) FI (Completed) DE (Completed) IT (Completed) BE (Completed) | ||
Trial results: View results |
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: 2013-002457-30 | Sponsor Protocol Number: 13.0099 | Start Date*: 2013-09-13 | |||||||||||||||||||||
Sponsor Name:St George's University of London | |||||||||||||||||||||||
Full Title: An open label randomised controlled trial investigating the effect of donepezil on regional cerebral blood flow in adults with aneurysmal subarachnoid haemorrhage. | |||||||||||||||||||||||
Medical condition: Aneurysmal subarachnoid haemorrhage Cerebral vasospasm Ischaemic stroke | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006785-29 | Sponsor Protocol Number: AC-054-302 | Start Date*: 2009-09-15 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group study to assess the efficacy and safety of clazosentan in reducing vasospasm-related morbidity and all-caus... | |||||||||||||
Medical condition: Indication: Subarachnoid aneurysmal hemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) FI (Prematurely Ended) AT (Prematurely Ended) BE (Completed) CZ (Completed) FR (Completed) DE (Completed) SI (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022874-15 | Sponsor Protocol Number: 10084 | Start Date*: 2010-11-08 |
Sponsor Name:University of Nottingham | ||
Full Title: Comparison of 30% nitrous oxide with therapeutic dose nimodipine on cerebral and systemic vascular physiology | ||
Medical condition: This is part of a series of studies investigating the potential therapeutic use of low dose nitrous oxide in the treatment of cerebral vasospasm, a condition which occurs following brain injury and... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004669-24 | Sponsor Protocol Number: 8103 | Start Date*: 2009-01-02 |
Sponsor Name:Research Innovation Services, University of Nottingham | ||
Full Title: Nitrous Oxide and Cerebral Autoregulation | ||
Medical condition: This study is being conducted to evaluate the effects of inhaled concentrations of 20%, 30% and 40% Nitrous Oxide on cerebral autoregulation in healthy volunteers using transcranial doppler ultraso... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002798-50 | Sponsor Protocol Number: prostacyclin | Start Date*: 2011-09-27 | |||||||||||
Sponsor Name:Rune Rasmussen | |||||||||||||
Full Title: Effect of prostacyclin infusion on cerebral vessels and metabolism in patients with subarachnoid haemorrhage | |||||||||||||
Medical condition: Vasospasm following subarachnoid hemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2007-007094-23 | Sponsor Protocol Number: Nitrous oxide protocol V5 | Start Date*: 2008-10-09 |
Sponsor Name:University of Nottingham | ||
Full Title: Nitrous oxide and cerebral vasodilatation: a dose-response study in healthy volunteers | ||
Medical condition: The study will be conducted in healthy volunteers. I will evaluate the effects of inhaled concentrations of nitrous oxide, ranging from 0% to 50%, on cerebral blood flow and cerebral vascular tone ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-018181-36 | Sponsor Protocol Number: 09117 | Start Date*: 2010-02-23 |
Sponsor Name:University of Nottingham | ||
Full Title: Nitrous Oxide and Functional Magnetic Resonance Imaging to investigate cerebral regional blood flow, cerebral metabolism and neuronal activity. | ||
Medical condition: This is part of a series of studies investigating the potential therapeutic use of low dose nitrous oxide in the treatment of cerebral vasospasm, a condition which occurs following brain injury and... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (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: 2018-003697-27 | Sponsor Protocol Number: CS2/713 | Start Date*: 2020-05-04 | |||||||||||
Sponsor Name:AOU CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO | |||||||||||||
Full Title: Effect of inhalatory sedation on cerebral perfusion in subarchnoid hemorrhage | |||||||||||||
Medical condition: Patients with non traumatic subarachnoid hemorrhage (WFNS = 3 -5) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000868-15 | Sponsor Protocol Number: P001151 | Start Date*: 2019-01-15 | |||||||||||
Sponsor Name:Medical Center -University of Freiburg | |||||||||||||
Full Title: Stereotactic Cisternal Lavage in Patients with Aneurysmal Subarachnoid Hemorrhage with Urokinase and Nimodipine for the Prevention of Secondary Brain Injury. A Randomized Controlled Trial. | |||||||||||||
Medical condition: Aneurysmal Subarachnoid Hemorrhage (aSAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002145-37 | Sponsor Protocol Number: 49RC19_0016 | Start Date*: 2019-12-26 | ||||||||||||||||
Sponsor Name:University Hospital of Angers (CHU d'Angers) | ||||||||||||||||||
Full Title: MIVAR - Milrinone Infusion for VAsospam treatment in subarachnoid hemoRrhage | ||||||||||||||||||
Medical condition: hémorragies méningées ou sous-arachnoïdiennes avec vasospasme | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001287-10 | Sponsor Protocol Number: NBK241/2/2022 | Start Date*: 2023-09-22 | |||||||||||
Sponsor Name:Gdański Uniwersytet Medyczny | |||||||||||||
Full Title: Treatment of acute ischemic stroke due to occlusion of a large vessel by mechanical thrombectomy in patients with unknown onset or not meeting the criteria for CT eligibility (ASPECTS <6) based on ... | |||||||||||||
Medical condition: acute ischemic stroke caused by occlusion of a large vessel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000768-27 | Sponsor Protocol Number: BAY59-7939/16573 | Start Date*: 2015-01-29 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Multicenter, randomized, double-blind, double-dummy, active-comparator, event-driven, superiority phase III study of secondary prevention of stroke and prevention of systemic embolism in patients w... | |||||||||||||
Medical condition: Embolic stroke of undetermined source (ESUS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) IE (Prematurely Ended) PT (Prematurely Ended) CZ (Completed) BE (Completed) ES (Completed) IT (Prematurely Ended) HU (Completed) FI (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
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