- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
58 result(s) found for: Atorvastatin (Lipitor).
Displaying page 1 of 3.
EudraCT Number: 2004-001994-24 | Sponsor Protocol Number: atorvastatin | Start Date*: 2004-11-09 |
Sponsor Name:Karolinska Institute Danderyd Hospital | ||
Full Title: Effects of atorvastatin on plasma fibrin gel structure and skin microvascular reactivity in patients with type 1 diabetes and dyslipidemia | ||
Medical condition: Hyperlipidemia in patients with diabetes seems associated with a thrombogenic plasma fibrin gel structure and impaired microvascular function. We hypothesize that lipid lowering with a statin leads... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003775-21 | Sponsor Protocol Number: ALH2 | Start Date*: 2008-08-14 |
Sponsor Name:Salford Royal Hospitals NHS Trust [...] | ||
Full Title: Effects of atorvastatin on microcirculatory endothelial function in patients with systemic sclerosis | ||
Medical condition: Systemic sclerosis (also termed 'scleroderma') | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004269-14 | Sponsor Protocol Number: A5091026 | Start Date*: 2005-02-21 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: Phase 3, Multi-center, double-blind, randomized, parallel group study of the efficacy, safety, and tolerability of fixed combination torcetrapib (CP-529,414)/Atorvastatin administered orally, once ... | |||||||||||||
Medical condition: Heterozygous Familial Hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000706-30 | Sponsor Protocol Number: A2581175 | Start Date*: 2012-02-09 |
Sponsor Name:Pfizer Inc | ||
Full Title: An Open Label, Randomized, Single Dose, Two-Way Crossover bioequivalence Study Comparing a New 80 mg (2x40 mg) Pediatric Appropriate Formulation to an 80 mg Commercial Atorvastatin Calcium Tablet F... | ||
Medical condition: pharmacokinetic trial | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-001198-18 | Sponsor Protocol Number: ITS2006-1 | Start Date*: 2006-05-30 |
Sponsor Name:Sligo General Hospital | ||
Full Title: Improving Tolerability of Statins | ||
Medical condition: Subjects for whom statin intake is a necessary therapeutic intervention i.e diabetics, dyslipidemics and patients with ischaemic heart disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005084-29 | Sponsor Protocol Number: 1 | Start Date*: 2006-03-23 |
Sponsor Name:Chief Scientitst Office | ||
Full Title: The effect of intensive lipid lowering on markers of inflammation in patients with stable coronary artery disease. | ||
Medical condition: Patients with cardiovascular risk factors and stable coronary artery disease, with a fasting total cholesterol level ≥5 mmol/l. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003584-31 | Sponsor Protocol Number: 85/2006 | Start Date*: 2006-08-31 |
Sponsor Name:Dept. Ob.Gyn, Univ Oulu | ||
Full Title: The effect of atorvastatin on insulin sensitivity, glucose metabolism and hormonal and inflammatory parameters in women with polycystic ovary syndrome (PCOS). | ||
Medical condition: Polycytic ovary syndrome (PCOS), | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000139-27 | Sponsor Protocol Number: A509 1018 | Start Date*: 2004-09-14 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: A Phase 3, Double-Blind, Placebo-Controlled, Randomized, Parallel Group, Multicenter Study of the Efficacy, Safety, and Tolerability of Fixed Combination Torcetrapib/Atorvastatin Administered Orall... | |||||||||||||
Medical condition: Mixed dyslipidemia (Frederickson Types IIa and IIb) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009334-32 | Sponsor Protocol Number: 07012009 | Start Date*: 2009-12-28 |
Sponsor Name:University medical center Utrecht | ||
Full Title: Effect of Statins on Sympathetic Activity in Hypertensive Patients with Chronic Kidney Disease: a Randomized trial in Hypertensive Patients with Chronic Kidney Disease | ||
Medical condition: atients older than 18 years old with stable chronic kidney disease and hypertension are included in this project. Patients with diabetes mellitus, patients on renal replacement therapy, patients on... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000728-17 | Sponsor Protocol Number: A2581174 | Start Date*: 2012-02-13 |
Sponsor Name:Pfizer Inc | ||
Full Title: An Open Label, Randomized, Single Dose, Two-Way Crossover Bioequivalence Study Comparing a Pediatric Appropriate Formulation to a 10 mg Commercial Atorvastatin Calcium Tablet Formulation in Healthy... | ||
Medical condition: pharmacokinetic | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2010-022040-20 | Sponsor Protocol Number: Statin_2010 | Start Date*: 2010-12-17 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: A Randomised Controlled Trial of Atorvastatin as an Anti-Inflammatory Agent in Non-Cystic Fibrosis Bronchiectasis | |||||||||||||
Medical condition: The aim of this randomised double blind controlled study to evaluate the efficacy of 6 months treatment with atorvastatin versus placebo in patients with clinically significant bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005703-42 | Sponsor Protocol Number: TMT106468 | Start Date*: 2006-03-29 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A 12 week, randomised, double blind study evaluating the effects of low dose (10mg) and high dose (80mg) atorvastatin on macrophage activity and carotid plaque inflammation as determined by Ultra s... | ||
Medical condition: Atherosclerotic Carotid Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000873-32 | Sponsor Protocol Number: RGHT000255 | Start Date*: 2006-08-02 |
Sponsor Name:Royal Group of Hospitals Trust | ||
Full Title: Effect of statin therapy on monocyte function in the metabolic syndrome. | ||
Medical condition: Metabolic syndrome, the essential feature of which is central obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-006497-17 | Sponsor Protocol Number: 0653A-107 | Start Date*: 2007-05-21 | |||||||||||
Sponsor Name:MSP Singapore Co., LLC c/o Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel Arm, 6-Week Study to Evaluate the Efficacy and Safety of Ezetimibe/Simvastatin Versus Atorvastatin in Patients with Metabolic Syndrome and Hypercho... | |||||||||||||
Medical condition: Hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) NL (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007689-52 | Sponsor Protocol Number: 0653A-133 | Start Date*: 2009-05-27 | |||||||||||
Sponsor Name:Merck & Co. Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Active-Controlled, Multicenter Study of Patients with Cardiovascular Disease and Diabetes Mellitus Not Adequately Controlled with Simvastatin 20 mg or Atorvastatin 10 mg... | |||||||||||||
Medical condition: Lipids not at goal in diabetic patients with cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) HU (Completed) DE (Completed) LV (Completed) AT (Completed) EE (Completed) IT (Completed) PT (Completed) BG (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005002-40 | Sponsor Protocol Number: 0653A-134 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: "Estudio aleatorizado, doble ciego, con control activo, multicéntrico en pacientes con hipercolesterolemia primaria y alto riesgo cardiovascular y no controlados adecuadamente con Atorvastatina 20 ... | |||||||||||||
Medical condition: hipercolesterolemia primaria primary hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) PT (Completed) LV (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022042-24 | Sponsor Protocol Number: Statin_p.aeruginosa | Start Date*: 2010-12-24 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: A Randomised Controlled Trial of Atorvastatin as an Anti-Inflammatory Agent in Non-Cystic Fibrosis Bronchiectasis in patients with Pseudomonas Aeruginosa | |||||||||||||
Medical condition: The aim of this randomized double blind controlled study is to evaluate the efficacy of a 3 months treatment with atorvastatin versus placebo in patients with clinically significant bronchiectasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003396-20 | Sponsor Protocol Number: MMUH-Conway01 | Start Date*: 2012-11-26 |
Sponsor Name:Cardiothoracic Surgery, Mater Misericordiae University Hospital | ||
Full Title: Is the optimal dose of preoperative statin associated with decreased end organ injury and better clinical outcome post cardiopulmonary bypass? | ||
Medical condition: Patient listed for open heart surgery involving cardiopulmonary bypass. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003684-41 | Sponsor Protocol Number: 6213-006-03 | Start Date*: 2007-11-01 |
Sponsor Name:MSD Finland Oy | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo- and Active- Controlled Study to Assess the Efficacy and Tolerability of MK-6213 Co-Administered With Atorvastatin in Patients with Primary Hypercho... | ||
Medical condition: Primary hypercholesterolemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) BE (Completed) DE (Completed) SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-004448-60 | Sponsor Protocol Number: 0653A-128 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel Arm, 12-Week Study to Evaluate the Efficacy and Safety of Ezetimibe/Simvastatin Combination Tablet Versus Atorvastatin in Elderly Patients With Hyp... | |||||||||||||
Medical condition: Hypercholesterolemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) IE (Completed) FI (Completed) BE (Completed) DK (Completed) DE (Completed) IT (Completed) AT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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