- Trials with a EudraCT protocol (248)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
248 result(s) found for: Clopidogrel.
Displaying page 1 of 13.
EudraCT Number: 2011-004748-23 | Sponsor Protocol Number: 2011080362 | Start Date*: 2011-12-05 |
Sponsor Name:Neurologisk Afdeling | ||
Full Title: Risk of apoplexia cerebri in clopidogrel non-responders. | ||
Medical condition: Apoplexia cerebri | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-003907-11 | Sponsor Protocol Number: ICP-2007/00 | Start Date*: 2008-01-30 |
Sponsor Name:Grupo de Investigación ICP | ||
Full Title: Estudio aleatorizado, unicéntrico, que compara un régimen de dosis elevada de clopidogrel frente a la dosis estándar en pacientes diabéticos tipo 2 revascularizados mediante una estrategia invasiv... | ||
Medical condition: Síndrome coronario agudo (angina inestable / infarto agudo de miocardio sin elevación de ST) en combinación con Ácido Acetilsalicílico | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003548-38 | Sponsor Protocol Number: 2015-1CR | Start Date*: 2015-09-29 | |||||||||||
Sponsor Name:Roskilde Hospital | |||||||||||||
Full Title: CLOpidogrel response and CYP2C19 Genotype in Ischemic Stroke patients | |||||||||||||
Medical condition: Ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001661-27 | Sponsor Protocol Number: ISSBRIL0162 | Start Date*: 2014-12-12 |
Sponsor Name:Sociedad Española de Cardiología | ||
Full Title: Comparison of TIcagrelor and clopidogrel in patients with Coronary artery diseaSe and type 2 Diabetes Mellitus (TICS-DM): a randomized pharmacodynamic study | ||
Medical condition: Coronary artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000942-11 | Sponsor Protocol Number: 140207 | Start Date*: 2008-04-30 |
Sponsor Name:Medizinische Universität Wien/ Universitätsklinik für Innere Medizin II/ Angiologie und Kardiologie | ||
Full Title: Vienna-Resistance to Antithrombotic Therapy (REACT) | ||
Medical condition: Resistance to Aspirin and Clopidogrel | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000754-40 | Sponsor Protocol Number: TUD-CLOPIS-009 | Start Date*: 2007-02-28 |
Sponsor Name:Dresden University of Technology | ||
Full Title: Interaktion von Statinen mit Clopidogrel als Sekundärprophylaxe bei der akuten zerebralen Ischämie - CLOPISTAT | ||
Medical condition: transitoric ischemic attack or cerebral ischemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022461-10 | Sponsor Protocol Number: Final Version1 | Start Date*: 2011-02-08 |
Sponsor Name:Southampton University Hospitals NHS Trust | ||
Full Title: A pilot study investigating the antiplatelet effect of generic clopidogrel versus Plavix™ – is there any difference in platelet reactivity in healthy subjects? | ||
Medical condition: The intended indication for the product is for use in all patients with acute coronary syndromes and following coronary artery stenting | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005292-15 | Sponsor Protocol Number: H7T-MC-TABR & TABR (1) | Start Date*: 2006-03-02 | |||||||||||
Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||
Full Title: A Pharmacokinetic and Pharmacodynamic Comparison of Prasugrel (LY640315) versus Clopidogrel in Subjects with Stable Atherosclerosis | |||||||||||||
Medical condition: Stable atherosclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002675-17 | Sponsor Protocol Number: TIGER-BVS | Start Date*: 2014-05-30 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
Full Title: Ticagrelor and absorb bioresorbable vascular scaffold implantation for recovery of vascular function after successful chronic total occlusion recanalization | ||
Medical condition: Chronic total coronary occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003733-25 | Sponsor Protocol Number: CHUBX2013/27 | Start Date*: 2014-12-03 |
Sponsor Name:CHU de BORDEAUX | ||
Full Title: Pilot Study related to the effect of clopidogrel on plasmatic soluble CD40 ligand during systemic lupus erythematous | ||
Medical condition: systemic lupus erythematous | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006611-29 | Sponsor Protocol Number: 80009 | Start Date*: 2022-06-28 |
Sponsor Name:University Medical Centre Utrecht Department of Vascular Surgery | ||
Full Title: A randomized placebo-controlled double-blind trial studying the effect of antiplatelet monotherapy (clopidogrel) versus dual antiplatelet therapy (clopidogrel + aspirin) on the occurrence of athero... | ||
Medical condition: (Chronic) Peripheral (occlusive) arterial disease (PAD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003125-28 | Sponsor Protocol Number: POPTAV001 | Start Date*: 2013-12-24 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: Antiplatelet therapy for patients undergoing transcatheter aortic valve implantation | ||
Medical condition: Aortic stenosis for which a transcatheter aortic valve implantation (TAVI) is performed. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020219-35 | Sponsor Protocol Number: | Start Date*: 2011-07-18 |
Sponsor Name:Royal Brompton & Harefield NHS Foundation Trust | ||
Full Title: Evaluating the benefit of additional platelet inhibition in acute coronary syndrome patients with high platelet reactivity undergoing PCI | ||
Medical condition: Cardiovascular disease - Acute coronary syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003621-33 | Sponsor Protocol Number: ESR-15-10793 | Start Date*: 2016-02-25 | |||||||||||
Sponsor Name:Fundación Interhospitalaria de Investigación Cardiovascular | |||||||||||||
Full Title: PRotective Effect on the coronary microcirculation of patients with DIabetes by Clopidogrel or Ticagrelor:A randomized multicenter clinical trial using intracoronary multimodal physiology | |||||||||||||
Medical condition: Ischemic Heart Disease in Diabetic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001245-89 | Sponsor Protocol Number: BDR4580 | Start Date*: 2015-04-13 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Relative bioavailability study between 75 mg tablet and 75 mg solution of Clopidogrel (SR25990C) after single oral administration to young healthy men. Open, crossover, randomized and monocenter study | |||||||||||||
Medical condition: Young healthy men (intended indication cardiovascular disease) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000517-19 | Sponsor Protocol Number: 00/04/02 | Start Date*: 2005-11-23 |
Sponsor Name:Blackpool Fylde & Wyre Healthcare NHS Trust | ||
Full Title: PRETREATMENT WITH HIGH DOSE CLOPIDOGREL FOR REDUCTION OF THROMBOTIC EVENTS AFTER ELECTIVE CORONARY TERRITORY STENTING WITH DRUG ELUTING STENTS: ThePROTECTED Study | ||
Medical condition: PERCUTANEOUS CORONARY INTERVENTION( USING DRUG ELUTING STENTS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005305-19 | Sponsor Protocol Number: D5130C00030 | Start Date*: 2008-11-17 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomised, Double-Blind, Outpatient, Crossover Study of the Anti-platelet Effects of AZD6140 Compared with Clopidogrel in Patients with Stable Coronary Artery Disease Previuosly Identified as Cl... | |||||||||||||
Medical condition: Stable Coronary Artery Disease AZD6140 is under development for the prevention of thrombotic events in patients with non-ST and ST elevation coronary syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000658-27 | Sponsor Protocol Number: D5130C05262 | Start Date*: 2006-12-12 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomised, Double-blind, Parallel Group, Phase 3, Efficacy and Safety Study of AZD6140 Compared with Clopidogrel for Prevention of Vascular Events in Patients with Non-ST or ST Elevation Acute C... | |||||||||||||
Medical condition: non-ST and ST elevation acute coronary syndromes (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) PT (Completed) HU (Completed) DE (Completed) FR (Completed) SE (Completed) AT (Completed) NL (Completed) DK (Completed) SK (Completed) BE (Completed) CZ (Completed) GR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003698-25 | Sponsor Protocol Number: RHMMED1063 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: Proof of concept clinical trial examining the effect of clopidogrel on allergen challenge in asthma | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000313-20 | Sponsor Protocol Number: 1208094 | Start Date*: 2013-06-14 | |||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||
Full Title: Evaluation of the biological response to clopidogrel in patients with ischemic stroke: role of platelet alpha2-adrenergic receptors | |||||||||||||
Medical condition: Ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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