- Trials with a EudraCT protocol (27)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
27 result(s) found for: Arachidonic acid.
Displaying page 1 of 2.
EudraCT Number: 2018-000017-20 | Sponsor Protocol Number: ASS-Metamizol-DDI | Start Date*: 2018-07-17 |
Sponsor Name:Universitäts-Herzzentrum Freiburg • Bad Krozingen | ||
Full Title: Antiplatelet effect of acetylsalicylic acid in patients after cardiac surgery: Impact of dipyrone (metamizole) | ||
Medical condition: Antithrombotic therapy after surgical replacement of stenotic heart valve by a bioprosthesis or mitral valve repair | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004814-33 | Sponsor Protocol Number: MOFA | Start Date*: 2006-03-23 |
Sponsor Name:Gesellschaft für Wissens- und Technologietransfer | ||
Full Title: Metabolic optimized fast track concept in general surgery | ||
Medical condition: Carcinoma of the colon or the liver scheduled for surgical resection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000920-25 | Sponsor Protocol Number: STH19177 | Start Date*: 2016-04-15 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A study of very low dose twice-daily compared to standard low dose once-daily aspirin following acute coronary syndromes - WILL lOWer dose aspirin be more effective following ACS? | |||||||||||||
Medical condition: Acute coronary syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002233-19 | Sponsor Protocol Number: ASA-CABG-01 | Start Date*: 2011-10-14 |
Sponsor Name:Karolinska Institute | ||
Full Title: Antiplatelet effects of once versus twice daily dosing of aspirin after coronary artery bypass grafting | ||
Medical condition: Patients having successfully undergone coronary artery bypass graft (CABG) surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000499-89 | Sponsor Protocol Number: DK0100 | Start Date*: 2015-11-09 |
Sponsor Name:Royal College Of Surgeons Ireland | ||
Full Title: To measure the effects of Aspirin loading dose of 300mgs in healthy controls using AA LTA and the Dynamic Platelet Function Assay (DPFA). | ||
Medical condition: Cardiovascular disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004208-11 | Sponsor Protocol Number: Kozek200701 | Start Date*: 2008-04-28 |
Sponsor Name:Medizinische Universität Wien, Univ.-Klinik für Spezielle Anästhesie und Schmerztherapie | ||
Full Title: Effect of chronic garlic intake on platelet function | ||
Medical condition: improvement in overall health status by garlic and preoperative setting | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003186-40 | Sponsor Protocol Number: DM-ASA 001 | Start Date*: 2007-09-05 |
Sponsor Name:Karolinska Institute | ||
Full Title: Evaluation of antiplatelet effects of different dosages of aspirin in type 2 diabetic patients. | ||
Medical condition: Patients with type 2 diabetes mellitus with an indication for aspirin treatment or already on aspirin treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003611-21 | Sponsor Protocol Number: 2013-003611-21 | Start Date*: 2013-12-20 | ||||||||||||||||
Sponsor Name:Karolinska Institutet | ||||||||||||||||||
Full Title: Safety of fluconazol treatment of premature and full-term newborns - a study on interactions by NSAIDs with fluconazole in respect of pharmacodynamic endpoints with urinary excretion of vas... | ||||||||||||||||||
Medical condition: Fungal infection prophylaxis Patent ductus arteriosus | ||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000614-21 | Sponsor Protocol Number: 7168K01 | Start Date*: 2007-08-09 | |||||||||||
Sponsor Name:Zambon Group S.p.A | |||||||||||||
Full Title: A multicentre, open-label study to evaluate the efficacy and safety of 5-MTHF administration, added on to the individual established therapy, on plasma homocysteine levels in patients with congenit... | |||||||||||||
Medical condition: homocystinuria | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) HU (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002226-76 | Sponsor Protocol Number: 6.1 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | |||||||||||||
Full Title: High “on treatment” platelet reactivity in the Intensive Care Unit | |||||||||||||
Medical condition: mixed medical intensive care unit patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004772-19 | Sponsor Protocol Number: 04122019 | Start Date*: 2020-04-08 |
Sponsor Name:Steno Diabetes Center Copenhagen | ||
Full Title: Platelet aggregation and aspirin low response in type one diabetes and the association with vascular damage and diabetic nephropathy | ||
Medical condition: Prevention of cardiovascular disease in persons with type 1 diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024064-18 | Sponsor Protocol Number: OM-EPA-003 | Start Date*: 2011-03-22 | |||||||||||
Sponsor Name:Omthera Pharmaceutical Inc. | |||||||||||||
Full Title: Efficacy and Safety of Epanova® in Severe Hypertriglyceridemia | |||||||||||||
Medical condition: Severe hypertriglyceridemia defined as serum triglyceride (TG) values ≥500 and <2000 mg/dL (≥5.65 mmol/L and <22.60 mmol/L). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002734-20 | Sponsor Protocol Number: CS/2014/4525 | Start Date*: 2014-10-23 | ||||||||||||||||
Sponsor Name:Research and Innovation Department | ||||||||||||||||||
Full Title: A Randomised Controlled Trial Investigating the Pharmacodynamic Effect of Ticagrelor Monotherapy on Platelet Reactivity in Patients with Coronary Artery Disease: The TEMPLATE Study | ||||||||||||||||||
Medical condition: Coronary artery disease previously treated with coronary stenting | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005779-86 | Sponsor Protocol Number: GFT505-208-3 | Start Date*: 2008-12-26 | ||||||||||||||||
Sponsor Name:GENFIT | ||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy and Safety of GFT505 (80 mg) orally administered once daily for 28 days in atherogenic dyslipidaemic patients with abdominal obesity. A double blind, placebo-... | ||||||||||||||||||
Medical condition: Atherogenic dyslipidaemic patients with abdominal obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020464-38 | Sponsor Protocol Number: PRENU | Start Date*: 2010-06-08 |
Sponsor Name:University of Oslo | ||
Full Title: Nutrition, growth and development among very preterm infants | ||
Medical condition: The main purpose of this study is to evaluate the effect of increased supply of energy, protein, vitamin A and the long chain polyunsaturated fatty acids DHA and AA to Very Low Birth Weight Infants... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000997-53 | Sponsor Protocol Number: RF-2009-1546106 | Start Date*: 2012-05-25 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: ANTIPLATELET TREATMENT FOR PREVENTION OF VASCULAR OUTCOMES IN PAD PATIENTS UNDERGOING PERIPHERAL REVASCULARIZATION. | |||||||||||||
Medical condition: Will be enrolled in the study patients suffering from intermittent claudication in whom resulted ineffective both pharmacological and workout therapy- Will be considered eligible patients aged 40-8... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003700-31 | Sponsor Protocol Number: ImNuT | Start Date*: 2017-10-11 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Effects of nutrition therapy on growth, metabolism and inflammation in immature infants; a double-blind randomized, controlled trial | ||
Medical condition: To determine whether early and prolonged supply of ARA and DHA improves quality of growth and clinical outcomes in extreme premature infants as compared to our present nutrient supply. By closely a... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000267-25 | Sponsor Protocol Number: STH20412 | Start Date*: 2020-03-17 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Characterisation of a novel regimen of very low-dose aspirin combined with rivaroxaban in patients with chronic coronary syndromes: WILL lOWer dose aspirin be better with rivaroxaban in patients wi... | |||||||||||||
Medical condition: Chronic coronary syndrome | |||||||||||||
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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: 2018-004285-34 | Sponsor Protocol Number: STH20370 | Start Date*: 2019-01-18 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The impact of aspirin dose modification on the innate immune response - WILL lOWer dose aspirin Therapy ReducE the response to Endotoxin? – (WILLOW TREE) | |||||||||||||
Medical condition: Acute coronary syndrome | |||||||||||||
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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: 2005-006026-28 | Sponsor Protocol Number: A3481066 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: Randomized, Double-Blind Study of the morphine-sparing efficacy and safety of Parecoxib sodium 40 mg i.v. followed by 20 mg i.v. every 12 hours in the treatment of pain following radical prostatectomy | |||||||||||||
Medical condition: Patients who are scheduled to undergo routine radical prostatectomy performed under a standardized regimen of general anesthesia, and who are expected to experience moderate to severe postsurgical ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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