- Trials with a EudraCT protocol (182)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (664)
182 result(s) found for: TIA.
Displaying page 8 of 10.
EudraCT Number: 2012-004494-23 | Sponsor Protocol Number: MAG104615 | Start Date*: 2013-03-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study MAG104615, a Proof of Concept Study for GSK249320 versus placebo in Stroke Patients | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003444-24 | Sponsor Protocol Number: 1160.189 | Start Date*: 2014-11-21 | ||||||||||||||||||||||||||
Sponsor Name:Unilfarma - União Internacional de Lab. Farmacêuticos, Lda. | ||||||||||||||||||||||||||||
Full Title: Randomized, double-blind, Evaluation in secondary Stroke Prevention comparing the EfficaCy and safety of the oral Thrombin inhibitor dabigatran etexilate (110 mg or 150 mg, oral b.i.d.) versus acet... | ||||||||||||||||||||||||||||
Medical condition: A study to compare dabigatran etexilate to acetylsalicylic acid in preventing recurrent stroke for patients that already had a stroke caused by an embolus (clot). Despite testing, it is unknown wh... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) HU (Completed) IT (Completed) SE (Completed) SI (Completed) ES (Completed) CZ (Completed) SK (Completed) PL (Completed) HR (Completed) GR (Completed) EE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002532-12 | Sponsor Protocol Number: IDE:G050233 | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:MAYO CLINIC | |||||||||||||
Full Title: Catheter Ablation Versus Antiarrhythmic Drug Therapy for Atrial Fibrillation Trial (CABANA) | |||||||||||||
Medical condition: Atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018421-19 | Sponsor Protocol Number: PASS | Start Date*: 2010-05-05 | ||||||||||||||||
Sponsor Name:AMC | ||||||||||||||||||
Full Title: Preventive Antibiotics in Stroke Study | ||||||||||||||||||
Medical condition: Stroke and stroke-associated infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006118-15 | Sponsor Protocol Number: CLAF237ADE07 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Multicentric cross-over trial to assess the glycemic profiles on 8 weeks of vildagliptin and sitagliptin treatment, each, in type-2 diabetic patients with a pre-existing cardiovascular disease pre-... | |||||||||||||
Medical condition: type-2 diabetes mellitus with pre-existing cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001967-22 | Sponsor Protocol Number: P01799 | Start Date*: 2014-08-05 | ||||||||||||||||
Sponsor Name:Papworth Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: A phase II study to investigate the protective effects of Glucagon-like Peptide-1 (GLP-1) in patients undergoing elective angioplasty and stenting. | ||||||||||||||||||
Medical condition: To determine whether an infusion of GLP1 can reduce the occurrence of myocyte necrosis and infarction caused by percutaneous coronary intervention | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001279-19 | Sponsor Protocol Number: SONAS2018 | Start Date*: 2019-08-19 | |||||||||||
Sponsor Name:BURL Concepts, Inc. | |||||||||||||
Full Title: Evaluation of the SONAS® ultrasound device for the assessment of bilateral cerebral perfusion in subjects with acute stroke | |||||||||||||
Medical condition: Acute large vessel occlusion (LVO) stroke (NIHSS score: ≥ 10) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011003-23 | Sponsor Protocol Number: GFT505-209-4 | Start Date*: 2009-05-28 | ||||||||||||||||
Sponsor Name:GENFIT | ||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy and Safety of GFT505 (80mg) orally administered once daily for 35 days in patients presenting with impaired glucose tolerance and abdominal obesity. A double ... | ||||||||||||||||||
Medical condition: patients presenting with impaired glucose tolerance and abdominal obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001723-36 | Sponsor Protocol Number: D1250C0051 | Start Date*: 2007-10-16 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A controlled, randomized, parallel, multi-centre, feasibility study of the oral direct thrombin inhibitor AZD0837, given as extended-release formulation, in the prevention of stroke and systemic em... | |||||||||||||
Medical condition: This is a phase II study to evaluate the feasibility of conducting a study in patients with AF who are appropriate for, but unable or unwilling to take VKA therapy. The intended indication for th... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012086-66 | Sponsor Protocol Number: T05018-1001 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:Grifols Inc | |||||||||||||
Full Title: A Phase 1/2a, Open Label, Dose Escalation, Safety Study of Intra-thrombus Plasmin (Human) Administration in Acute, Middle Cerebral Artery, Ischemic Stroke | |||||||||||||
Medical condition: Thrombus in acute ischemic stroke of the middle cerebral artery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) FR (Completed) SK (Completed) AT (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2017-001834-25 | Sponsor Protocol Number: MasterDapt | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:ECRI-9 | |||||||||||||
Full Title: MAnagement of high bleeding risk patients post bioresorbable polymer coated STEnt implantation with an abbReviated versus prolonged DAPT regimen – MASTER DAPT | |||||||||||||
Medical condition: High bleeding risk population represents a significant proportion of coronary artery disease (CAD) patients undergoing coronary stent implantation. Decisions regarding the duration of dual antiplat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) SE (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002442-45 | Sponsor Protocol Number: AXAFA-AFNET5 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Kompetenznetz Vorhofflimmern e.V. [Atrial Fibrillation NETwork (AFNET)] | ||||||||||||||||||||||||||||
Full Title: Anticoagulation using the direct factor Xa inhibitor apixaban during Atrial Fibrillation catheter Ablation: Comparison to vitamin K antagonist therapy. | ||||||||||||||||||||||||||||
Medical condition: Atrial fibrillation catheter ablation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) DK (Completed) GB (Completed) NL (Completed) ES (Completed) AT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003351-12 | Sponsor Protocol Number: A6141079 | Start Date*: 2005-10-27 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: The effect of eplerenone versus placebo on cardiovascular mortality and heart failure hospitalization in subjects with NYHA Class II Chronic Systolic Heart Failure | |||||||||||||
Medical condition: Chronic systolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) IE (Completed) SK (Completed) SE (Completed) GB (Completed) ES (Completed) HU (Completed) BE (Completed) PT (Completed) GR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004393-22 | Sponsor Protocol Number: LIB003-006 | Start Date*: 2022-01-13 | |||||||||||
Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Long-Term Efficacy and Safety of LIB003 in Patients With Cardiovascular Disease, or at High Risk for Cardiovascular Disea... | |||||||||||||
Medical condition: Patients With Cardiovascular Disease or at High Risk for Cardiovascular Disease, on Stable Lipid-Lowering Therapy Requiring Additional Low-Density Lipoprotein Cholesterol Reduction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001518-39 | Sponsor Protocol Number: K-877-303 | Start Date*: 2017-01-16 | |||||||||||
Sponsor Name:Kowa Research Institute, Inc. | |||||||||||||
Full Title: A Phase 3, Multi-Center, Placebo-Controlled, Randomized, Double-Blind, 12-Week Study With a 40-Week, Active-Controlled, Open-Label Extension to Evaluate the Efficacy and Safety of K-877 in Adult Pa... | |||||||||||||
Medical condition: Severe hypertriglyceridemia [fasting TG levels >=500 mg/dL (5.65 mmol/L) and <2000 mg/dL (22.60 mmol/L) and mild or moderate renal impairment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) BG (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001953-33 | Sponsor Protocol Number: PrevSVD-2015 | Start Date*: 2015-10-09 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||||||||||||||||||||||
Full Title: Preventing cognitive decline and dementia from cerebral small vessel disease | |||||||||||||||||||||||||||||||||
Medical condition: Lacunar (small vessel) ischaemic stroke | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005749-18 | Sponsor Protocol Number: B01-02 | Start Date*: 2013-08-29 | |||||||||||||||||||||
Sponsor Name:Athersys, Inc | |||||||||||||||||||||||
Full Title: Double-Blind, Randomized, Placebo-Controlled, Phase 2 Safety and Efficacy Trial of MultiStem® in Adults With Ischemic Stroke | |||||||||||||||||||||||
Medical condition: acute ischemic stroke | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003511-37 | Sponsor Protocol Number: K-877-301 | Start Date*: 2017-01-16 | |||||||||||
Sponsor Name:Kowa Research Institute, Inc. | |||||||||||||
Full Title: A Phase 3, Multi-Center, Placebo-Controlled, Randomized, DoubleBlind, 12-Week Study With a 40-Week, Active-Controlled, DoubleBlind Extension to Evaluate the Efficacy and Safety of K-877 in Adult ... | |||||||||||||
Medical condition: severe hypertriglyceridemia [fasting TG levels >=500 mg/dL (5.65 mmol/L) and <2000 mg/dL (22.60 mmol/L) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016057-17 | Sponsor Protocol Number: 23349 | Start Date*: 2011-07-14 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gentofte Hospital | ||||||||||||||||||||||||||||||||||||||
Full Title: Behandling med nerveaktiverende medicin efter apopleksi - måling af genoptræningseffekt, patologisk træthed, muskelstyrke og knogleafkalkning | ||||||||||||||||||||||||||||||||||||||
Medical condition: Apopleksi. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001757-21 | Sponsor Protocol Number: ESH-CHL-SHOT | Start Date*: 2013-05-21 | |||||||||||
Sponsor Name:ISTITUTO AUXOLOGICO ITALIANO | |||||||||||||
Full Title: European Society of Hypertension and Chinese Hypertension League stroke in hypertension optimal treatment trial | |||||||||||||
Medical condition: Patients with arterial hypertension and previous stroke or transient ischemic attack | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SE (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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