- Trials with a EudraCT protocol (95)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
95 result(s) found for: Nervous System Diseases AND Cardiovascular Diseases.
Displaying page 3 of 5.
EudraCT Number: 2015-005689-40 | Sponsor Protocol Number: COL-MIG-302 | Start Date*: 2016-10-18 | |||||||||||||||||||||||||||||||
Sponsor Name:CoLucid Pharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Study of Three Doses of Lasmiditan (50 mg, 100 mg and 200 mg) Compared to Placebo in the Acute TReaTment of MigrAiNe: A randomized, double-blind, placebo-controlled parallel group study (SPARTAN) | |||||||||||||||||||||||||||||||||
Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005317-37 | Sponsor Protocol Number: THR-2010-01 | Start Date*: 2012-06-14 | |||||||||||
Sponsor Name:Thrombotech Ltd. | |||||||||||||
Full Title: Double blind, placebo controlled, escalating single-dose, pilot study to assess the safety of THR-18 when administered to patients suffering acute ischemic stroke and treated with tPA | |||||||||||||
Medical condition: Acute isquemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003587-39 | Sponsor Protocol Number: COMBAT-MS | Start Date*: 2017-05-22 |
Sponsor Name:Karolinska Institutet | ||
Full Title: COMBAT-MS (COMparison Between All immunoTherapies for Multiple Sclerosis) A prospective long-term cohort study of safety, efficacy and patient’s satisfaction of MS disease modulatory treatments in... | ||
Medical condition: Relapsing-remitting multiple sclerosis (RRMS) that has started on their first or second immunomodulatory drug at the earliest 2011-01-01 and at the latest 2018-06-30. The clinical course and respon... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000075-85 | Sponsor Protocol Number: I-StrokeII2016 | Start Date*: 2018-06-19 | ||||||||||||||||
Sponsor Name:Karolinska Institutet | ||||||||||||||||||
Full Title: A phase 3, randomised, double-blind, placebo-controlled, parallel-arm efficacy trial of Imatinib in acute ischaemic stroke | ||||||||||||||||||
Medical condition: Patients with acute ischaemic stroke and an imaging scan excluding any intracranial haemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002211-18 | Sponsor Protocol Number: CAMG334A2301 | Start Date*: 2016-10-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-week double-blind, randomized, multicenter study comparing the efficacy and safety of once monthly subcutaneous 140 mg AMG 334 against placebo in adult episodic migraine patients who have fail... | |||||||||||||
Medical condition: Migraine Prevention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) SE (Completed) DE (Completed) FI (Completed) ES (Completed) AT (Completed) DK (Completed) BE (Completed) GR (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004919-43 | Sponsor Protocol Number: STOP-VD | Start Date*: 2014-05-14 | |||||||||||||||||||||
Sponsor Name:SOD Medicina e Cardiologia Geriatrica, Centro per lo Studio della Sincope - Università degli Studi di Firenze-AOUCareggi | |||||||||||||||||||||||
Full Title: Suspension of vasoactive drugs in reflex vasodepressive syncope: a randomized controlled trial | |||||||||||||||||||||||
Medical condition: Vasodepressive neuroreflex syncope | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000514-35 | Sponsor Protocol Number: Protect-U | Start Date*: 2018-04-04 | |||||||||||
Sponsor Name:Ruprecht-Karls-University Heidelberg, Medical Faculty Mannheim | |||||||||||||
Full Title: Prospective Randomised Open-label Trial to Evaluate risk faCTor management in patients with Unruptured intracranial aneurysms (PROTECT-U) | |||||||||||||
Medical condition: Saccular cerebral aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000494-36 | Sponsor Protocol Number: AC-083-103 | Start Date*: 2017-07-26 |
Sponsor Name:Idorsia Pharmaceuticals Ltd | ||
Full Title: A Phase 2a, multi-center, single-blind, within-subject, placebo-controlled study to assess the pharmacodynamics of ACT-709478 in subjects with photosensitive epilepsy | ||
Medical condition: Photosensitive epilepsy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002188-13 | Sponsor Protocol Number: UoL001087 | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:University of Liverpool [...] | |||||||||||||
Full Title: Emergency Treatment with Levetiracetam or Phenytoin in Status Epilepticus in Children (EcLiPSE) – an open label randomised controlled trial | |||||||||||||
Medical condition: Convulsive Status Epilepticus | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002075-10 | Sponsor Protocol Number: GN14NE598 | Start Date*: 2016-09-21 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis 2 | |||||||||||||
Medical condition: Acute ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022579-68 | Sponsor Protocol Number: COR-1/02 | Start Date*: 2011-08-16 | |||||||||||
Sponsor Name:Corimmun GmbH | |||||||||||||
Full Title: COR-1, an anti-ß1 receptor antibody cyclopeptide in heart failure: a phase II, multicentre, randomised, double-blind and placebo-controlled study with parallel groups | |||||||||||||
Medical condition: Heart Failure, Dilated Cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016737-95 | Sponsor Protocol Number: ROSPREC | Start Date*: 2011-07-13 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: ROSuvastatin Pretreatment to Reduce Embolization during Carotid Artery Stenting | |||||||||||||
Medical condition: Asymptomatic carotid stenosis >80% in patients with baseline LDL cholesterol >120 mg/dL. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000277-30 | Sponsor Protocol Number: STASH01 | Start Date*: 2006-07-06 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust [...] | |||||||||||||
Full Title: Simvastatin in aneurysmal subarchnoid haemorrhage (STASH): a multicentre randomised controlled clinical phase III study | |||||||||||||
Medical condition: subarachnoid haemorrhage | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000203-16 | Sponsor Protocol Number: SOMCT02 | Start Date*: 2018-06-18 | |||||||||||
Sponsor Name:SOM Biotech | |||||||||||||
Full Title: Phase IIa, double-blind, randomized, placebo-controlled study of the efficacy and safety of SOM3335 in Huntington`s disease (HD) patients with chorea movements. | |||||||||||||
Medical condition: Chorea movements associated with Huntington's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004318-25 | Sponsor Protocol Number: NL63681.029.18 | Start Date*: 2019-04-16 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Early high-dose vitamin C in post-cardiac arrest syndrome. | |||||||||||||
Medical condition: Patients admitted to the Intensive Care after out-of-hospital cardiac arrest with return of spontaneous circulation, ventricular fibrillation or ventricular tachycardia as first registered cardiac ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003870-27 | Sponsor Protocol Number: RA2363 | Start Date*: 2008-10-08 |
Sponsor Name:University of Nottingham | ||
Full Title: ENOS: Efficacy of Nitric Oxide in Stroke. Estudio ENOS: Eficacia del óxido nítrico en el ictus | ||
Medical condition: Hipertensión en el ictus agudo | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) DK (Completed) SE (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001975-30 | Sponsor Protocol Number: BAY59-7939/17938 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Global multicenter, open-label, randomized, event-driven, active-controlled study comparing a rivAroxaban-based antithrombotic strategy to an antipLatelet-based strategy after transcatheter aortIc ... | |||||||||||||
Medical condition: Patients with severe aortic stenosis that require Transcatheter aortic valve replacement are at risk of thrombus formation. Rivaroxaban (oral-anticoagulant) may reduce this risk, without increasing... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) BE (Prematurely Ended) NO (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) SE (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004175-12 | Sponsor Protocol Number: B7931028 | Start Date*: 2019-10-01 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A PHASE 2B, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, MULTICENTER, DOSE RANGING STUDY TO EVALUATE THE EFFICACY AND SAFETY PROFILE OF PF-06700841 IN PARTICIPANTS WITH ACTIVE SYSTEMIC LUPUS ERYTH... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) RO (Completed) BG (Completed) PT (Completed) DE (Completed) PL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001866-39 | Sponsor Protocol Number: NOE-TGN-201 | Start Date*: 2022-02-24 | |||||||||||
Sponsor Name:Noema Pharma | |||||||||||||
Full Title: A Phase II/III, multicentre, 8-week run-in phase followed by a 12- week, prospective, parallel-group, double-blind, randomized withdrawal, placebo-controlled study, with a 52 week open label exten... | |||||||||||||
Medical condition: Trigeminal neuralgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DK (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000619-26 | Sponsor Protocol Number: BAY59-7939/16416 | Start Date*: 2014-06-11 | ||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||||||||||||
Full Title: Reduced-dosed rivaroxaban and standard-dosed rivaroxaban versus ASA in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis and... | ||||||||||||||||||||||||||||
Medical condition: Long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis and/or pulmonary embolism | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) SE (Completed) AT (Completed) IT (Completed) ES (Completed) GB (Completed) CZ (Completed) DE (Completed) HU (Completed) DK (Completed) NL (Completed) NO (Completed) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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