- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: National Institutes of Health Stroke Scale.
Displaying page 1 of 3.
EudraCT Number: 2018-004325-88 | Sponsor Protocol Number: NTA1127 | Start Date*: 2019-03-11 |
Sponsor Name:Monash University - Eastern Health Clinical School | ||
Full Title: A multicentre, randomised controlled Trial of Exenatide versus standard care in Acute Ischemic Stroke (TEXAIS) | ||
Medical condition: Acute ischaemic stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003482-18 | Sponsor Protocol Number: RN01-CP-0002 | Start Date*: 2014-03-24 | |||||||||||
Sponsor Name:ReNeuron Ltd | |||||||||||||
Full Title: A Phase II Efficacy Study of Intracerebral CTX0E03 DP In Patients with Stable Paresis of the Arm Following an Ischaemic Stroke. | |||||||||||||
Medical condition: Supratentorial ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004681-16 | Sponsor Protocol Number: NTI-ASP-0502 | Start Date*: 2006-04-24 |
Sponsor Name:Neurobiological Technologies Inc | ||
Full Title: ASP I (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment within 6 Hour... | ||
Medical condition: Acute Ischemic Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2005-006067-31 | Sponsor Protocol Number: NTI-ASP-0503 | Start Date*: 2008-04-04 |
Sponsor Name:Neurobiological Technologies Inc | ||
Full Title: ASP II (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment within 6 Hou... | ||
Medical condition: Acute Ischemic Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) AT (Prematurely Ended) SK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005242-41 | Sponsor Protocol Number: RF-2019-12370834 | Start Date*: 2021-02-12 | |||||||||||
Sponsor Name:AZIENDA USL DI BOLOGNA | |||||||||||||
Full Title: FIBRINOGEN REPLACEMENT TO PREVENT INTRACRANIAL HAEMORRHAGE IN ISCHEMIC STROKE PATIENTS AFTER THROMBOLYSIS: A PILOT PROBE RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Ischemic stroke patients with secondary post-rtPA hypofibrinogenemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2004-002437-39 | Sponsor Protocol Number: SPI-103 | Start Date*: 2004-12-21 |
Sponsor Name:Daiichi Asubio Pharmaceuticals Inc. | ||
Full Title: A Phase IIb Randomized, Double-Blind, Placebo-Controlled, Group-Sequential, Multicenter, Dose Finding Study of the Safety and Efficacy of SUN N4057 (Piclozotan)Administered for 72 Hours by Continuo... | ||
Medical condition: Treatment of acute stroke. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) ES (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000421-34 | Sponsor Protocol Number: PN01-01/CD 003 | Start Date*: 2005-09-20 | |||||||||||
Sponsor Name:PAION Deutschland GmbH | |||||||||||||
Full Title: DESMOTEPLASE (INN) IN ACUTE ISCHAEMIC STROKE: PHASE III; A prospective, randomised, double-blind, placebo-controlled, single bolus, multinational, multi-centre, parallel group, dose ranging study o... | |||||||||||||
Medical condition: acute ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) AT (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019014-25 | Sponsor Protocol Number: Istrokepilot | Start Date*: 2010-07-27 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: A PROSPECTIVE, RANDOMISED, OPEN, BLINDED EVALUATION, ASCENDING-DOSE, PILOT TRIAL OF IMATINIB IN ACUTE ISCHAEMIC STROKE (I-STROKE/pilot) | ||
Medical condition: Acute ischaemic stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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: 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: 2010-021437-30 | Sponsor Protocol Number: PAISII-V01 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:ErasmusMC | |||||||||||||
Full Title: Paracetamol (Acetaminophen) in Stroke 2 (PAIS 2): A randomized, placebo-controlled clinical trial of high-dose paracetamol in patients with acute stroke and a body temperature of 36.5°C or above | |||||||||||||
Medical condition: acute stroke (cerebral infarction or intracrebral hemorrhage) and a body temperature of 36.5 degrees or above. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001592-37 | Sponsor Protocol Number: F02695_LP_2_05 | Start Date*: 2012-10-16 | |||||||||||
Sponsor Name:Pierre Fabre Médicament; Represented by Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: Effect of 3-month treatment with F2695 (75mg OD) on improving functional recovery of patients with ischemic stroke. A Multicenter, Randomised, Double-blind, Parallel-group, Placebo-Controlled Study. | |||||||||||||
Medical condition: Functionnal impairment after acute ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) PT (Completed) HU (Completed) BE (Completed) IT (Completed) FR (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003753-29 | Sponsor Protocol Number: M19-148 | Start Date*: 2020-05-14 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Proof-of-Concept Study to Assess the Safety and Efficacy of Elezanumab in Acute Ischemic Stroke | |||||||||||||
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: 2013-001757-28 | Sponsor Protocol Number: 2013/066st | Start Date*: 2013-11-20 | |||||||||||
Sponsor Name:Salford Royal NHS Foundation Trust | |||||||||||||
Full Title: Does subcutaneous interleukin-1 receptor antagonist reduce inflammation following ischaemic stroke compared to placebo? | |||||||||||||
Medical condition: Ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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 |
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: 2013-001617-32 | Sponsor Protocol Number: MINOR | Start Date*: 2013-12-05 |
Sponsor Name:AUSL di Piacenza | ||
Full Title: Thrombolysis in Minor Stroke | ||
Medical condition: The condition to be treated is the stroke of “minor” grade (National Institutes of Health Stroke Scale (NIHSS) score < 5). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002135-15 | Sponsor Protocol Number: CMMo/ICTUS/2013 | Start Date*: 2014-10-20 | |||||||||||
Sponsor Name:Iniciativa Andaluza en Terapias Avanzadas a través de la Fundación Progreso y Salud | |||||||||||||
Full Title: Opened phase II controlled and randomized clinical trial to evaluate the efficacy in the intra-arterial infusion with mononuclear autologous bone marrow stem cells in patients with ischemic stroke | |||||||||||||
Medical condition: ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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