- Trials with a EudraCT protocol (196)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
196 result(s) found for: Carotid artery.
Displaying page 1 of 10.
EudraCT Number: 2009-018166-36 | Sponsor Protocol Number: XENON-2009 | Start Date*: 2010-03-18 | |||||||||||
Sponsor Name:CHU de Poitiers | |||||||||||||
Full Title: Evaluation de l’entretien de l’anesthésie générale sous Xénon comparé au Desflurane au cours de l’endartérectomie carotidienne, étude prospective, randomisée et comparative. | |||||||||||||
Medical condition: Carotid artery stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000929-59 | Sponsor Protocol Number: MultiH/BRA/708 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bracco ALTANA Pharma GmbH | |||||||||||||
Full Title: INTRAINDIVIDUAL CROSS-OVER STUDY TO COMPARE MULTIHANCE® AND MAGNEVIST® AT A DOSE OF 0.1 MMOL/KGBW IN CERVICO-CEREBRAL MR ANGIOGRAPHY AND CEREBRAL MR PERFUSION IMAGING AT 3 TESLA IN PATIENTS WITH CA... | |||||||||||||
Medical condition: Carotid artery stenosis and scheduled for MRA, for MR perfusion examination and for an elective stent treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002681-34 | Sponsor Protocol Number: 1 | Start Date*: 2007-09-28 | |||||||||||
Sponsor Name:St Georges Healthcare NHS Trust | |||||||||||||
Full Title: Dual antiplatelet therapy in the acute phase following stroke and TIA; which is the best regimen? | |||||||||||||
Medical condition: Symptomatic carotid artery stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021526-36 | Sponsor Protocol Number: LMU_Rad_MR_GadoMRA01 | Start Date*: 2011-04-07 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Dynamic and high-resolution MR angiography of the supraaortic vessels at 3 Tesla: Performance of Gadobutrol (Gadovist) in comparison to Gedobenate Dimeglumine (Multihance) and Gadoterate Meglumine ... | |||||||||||||
Medical condition: Supraaortic vessel disease; suspicion or proven carotid artery stenosis / stenoses | |||||||||||||
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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: 2014-003213-29 | Sponsor Protocol Number: SPh/02/2014 | Start Date*: 2015-03-02 | ||||||||||||||||
Sponsor Name:SciencePharma spółka z ograniczoną odpowiedzialnością sp. j. | ||||||||||||||||||
Full Title: A randomized, multicenter, open-label, two-arm, parallel, phase III study to evaluate the efficacy and safety of nicotinic acid administered in combination with simvastatin for 6 months in comparis... | ||||||||||||||||||
Medical condition: Inhibiting the progression of atherosclerosis in patients with carotid arteries stenosis and dyslipidemia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003669-24 | Sponsor Protocol Number: E-010-08-09 | Start Date*: 2008-12-03 | |||||||||||
Sponsor Name:Deutsches Krebsforschungszentrum | |||||||||||||
Full Title: Intra-individual cross-over comparison of MultiHance® and Vasovist® enhanced MRA of the Carotids | |||||||||||||
Medical condition: Patients with at least one stenosis of one carotid artery of at least 90% as confirmed by Doppler ultrasound or other radiological methods who are scheduled for i.a. DSA for clinical reasons (or wh... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023001-36 | Sponsor Protocol Number: BAY86-4875/14607 | Start Date*: 2011-04-26 | |||||||||||
Sponsor Name:Bayer Health Care AG | |||||||||||||
Full Title: Multicenter, open-label study to evaluate the safety and efficacy (by blinded reading) of contrast-enhanced magnetic resonance angiography (MRA) after a single intravenous injection of 0.1 mmol/k... | |||||||||||||
Medical condition: Subjects with known or suspected vascular disease of the supra-aortic vessels | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) SE (Completed) FR (Completed) IT (Completed) PL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001006-10 | Sponsor Protocol Number: Revacept/CS/02 | Start Date*: 2012-05-31 | |||||||||||
Sponsor Name:advanceCOR GmbH | |||||||||||||
Full Title: REVACEPT, AN INHIBITOR OF PLATELET ADHESION IN SYMPTOMATIC CAROTID STENOSIS: A PHASE II, MULTICENTRE; RANDOMISED, DOSE-FINDING, DOUBLE-BLIND AND PLACEBO-CONTROLLED SUPERIORITY STUDY WITH PARALLEL G... | |||||||||||||
Medical condition: Patients suffering from symptomatic carotid artery stenosis, transient ischemic attacks, amaurosis fugax or stroke and who presenting with microembolic signals. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016902-17 | Sponsor Protocol Number: CLINMEDINT001 | Start Date*: 2012-05-18 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA OSPEDALI RIUNITI UMBERTO I - G.M.LANCISI - G.SALESI | ||||||||||||||||||
Full Title: Direct renin inhibitor (aliskiren)and carotid plaques instability markers in hypertensive patients requiring carotid endoarterectomy | ||||||||||||||||||
Medical condition: Essential hypertension. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Temporarily Halted) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001053-44 | Sponsor Protocol Number: Carotis-Rivaroxaban_CEUS_001 | Start Date*: 2020-09-30 | |||||||||||
Sponsor Name:Rigshospitalet, Department of Vascular Surgery | |||||||||||||
Full Title: Stabilization of vulnerable atherosclerotic carotid plaques by Rivaroxaban as evaluated by 3D contrast enhanced ultrasound (CEUS) | |||||||||||||
Medical condition: Patients with - Stable peripheral artery disease and - Asymptomatic, atherosclerotic plaque/stenosis in the carotid artery; asymptomatic regarding cerebral ischaemia including stroke and transient... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005555-27 | Sponsor Protocol Number: ESR-14-10473 | Start Date*: 2017-09-12 |
Sponsor Name:University Hospital Basel | ||
Full Title: Prevention of Cerebral Ischaemia in Stent Treatment for Carotid Artery Stenosis - A randomised multi-centre phase II trial comparing Ticagrelor versus Clopidogrel with outcome assessment on MRI (PR... | ||
Medical condition: Carotid artery stenting (CAS) is treatment for atherosclerotic carotid stenosis. The main adverse events are thromboembolic brain infarcts during the procedure. Ticagrelor, a novel reversible inhib... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003470-88 | Sponsor Protocol Number: 11-195 | Start Date*: 2012-07-30 | ||||||||||||||||
Sponsor Name:University Medical Center Utrecht, The Netherlands | ||||||||||||||||||
Full Title: Phenylephrine versus EPhedrine on cerebral Perfusion during carotid EndarteRectomy: PEPPER study | ||||||||||||||||||
Medical condition: Hypotension during carotid endarterectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004209-27 | Sponsor Protocol Number: 05/Q1606/127 | Start Date*: 2005-11-11 |
Sponsor Name:Oxford Radcliffe Hospitals NHS Trust | ||
Full Title: Effect of altering inspired oxygen concentrations on cerebral oxygenation during awake carotid surgery | ||
Medical condition: Carotid endarterectomy is an operation performed on patients with a symptomatic stenosis of the internal carotid artery. Such patients have usually presented with stroke or transient ischaemic atta... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2008-005246-23 | Sponsor Protocol Number: ARC1779-008 | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:Archemix Corp. | |||||||||||||
Full Title: A Study of the Effect of ARC1779 Injection on Cerebral Microembolism in Patients Undergoing Carotid Endarterectomy | |||||||||||||
Medical condition: Patients undergoing carotid endarterectomy, | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003010-14 | Sponsor Protocol Number: CACZ885M2301S1 | Start Date*: 2013-01-23 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled, event-driven trial of quarterly subcutaneous canakinumab in the prevention of recurrent cardiovascular events among stable post-myocardial infarction... | ||
Medical condition: atherosclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) GB (Prematurely Ended) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000456-17 | Sponsor Protocol Number: 43466 | Start Date*: 2019-10-16 | |||||||||||
Sponsor Name:University Hospital Maastricht | |||||||||||||
Full Title: Plaque at risk (ParisK): Molecular imaging of plaque vulnerability using 18F-choline PET-CT and MRI in carotid artery atherosclerosis patients | |||||||||||||
Medical condition: Patients with carotid artery stenosis due to atherosclerosis, who are scheduled for carotid endarterectomy or are treated conservatively. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017725-19 | Sponsor Protocol Number: NC22703 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A Phase IIIB multicenter, double-blind, randomized, placebocontrolled study, evaluating the effect of treatment with dalcetrapib 600 mg on Atherosclerotic Disease as measured by I. Coronary Intrava... | |||||||||||||
Medical condition: A Study of the Effect of Dalcetrapib on Artherosclerotic Disease in Patients With Coronary Artery Disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007673-23 | Sponsor Protocol Number: 07/H0308/171 | Start Date*: 2008-03-12 | |||||||||||
Sponsor Name:Cambridge University Hospitals Foundation Trust | |||||||||||||
Full Title: Evaluation of carotid atheroma with contrast enhanced magnetic resonance imaging | |||||||||||||
Medical condition: Carotid artery atheroma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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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