- Trials with a EudraCT protocol (305)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
305 result(s) found for: Lipid metabolism.
Displaying page 1 of 16.
EudraCT Number: 2016-003551-30 | Sponsor Protocol Number: August2016 | Start Date*: 2017-03-02 | |||||||||||
Sponsor Name:Universitätsklinikum Freiburg | |||||||||||||
Full Title: Modeling of the impact of a PCSK9 inhibition on lipoproteins in patients with dyslipidemia | |||||||||||||
Medical condition: dyslipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007491-42 | Sponsor Protocol Number: 2418/2007 | Start Date*: 2008-01-21 | |||||||||||
Sponsor Name:Istituto Fisiologia Clinica, CNR | |||||||||||||
Full Title: GAMMAGLUTAMYLTRANSFERASE: CHARACTERIZATION OF ITS ISOFORMS IN DYSLIPIDEMICS UNDERGOING LIPID-LOWERING TREATMENT | |||||||||||||
Medical condition: Dislipidemiae (hypercholesteremia, hypertriglyceridemia or mixed forms) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002423-33 | Sponsor Protocol Number: BVT.BSSL-020 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:BIOVITRUM AB | |||||||||||||
Full Title: A prospective, randomised, double-blind crossover study comparing 0.15 g/L rhBSSL added to infant formula versus placebo during one week of treatment in preterm infants born before week 32 of gesta... | |||||||||||||
Medical condition: Enzyme replacement therapy in pre-term infants. Reduced fad uptake capabilities due to prematurity of pre-term infants | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002236-26 | Sponsor Protocol Number: P04037 | Start Date*: 2005-01-11 | |||||||||||
Sponsor Name:SCHERING-PLOUGH | |||||||||||||
Full Title: A Multicenter, Randomized, Parallel-Groups, Double-Blind Placebo Controlled Study Comparing The Efficacy, Safety, And Tolerability Of Co-administration Of Ezetimibe 10 Mg With Ongoing Treatment wit... | |||||||||||||
Medical condition: Primary Hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000824-20 | Sponsor Protocol Number: 239/2007 | Start Date*: 2008-06-15 | ||||||||||||||||||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | ||||||||||||||||||||||||||||
Full Title: Effects of ezetimibe in association with statins on postprandial lipemia in type 2 diabetic patients | ||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002434-10 | Sponsor Protocol Number: BVT.BSSL-021 | Start Date*: 2007-10-17 |
Sponsor Name:Biovitrum AB (publ.) | ||
Full Title: A prospective, randomised, double-blind crossover study comparing 0.15 g/L rhBSSL added to pasteurized breast milk versus placebo during one week of treatment in preterm infants born before week 32... | ||
Medical condition: Enzyme replacement therapy in pre-term infants. Reduced fat uptake capabilities due to prematurity of pre-term infants | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001205-27 | Sponsor Protocol Number: ABR35884 | Start Date*: 2011-08-04 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: The effect of fibrate therapy in two patients with neutral lipid storage disease with myopathy (NLSDM). | |||||||||||||||||||||||
Medical condition: Neutral lipid storage disease with myopathy | |||||||||||||||||||||||
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Population Age: | Gender: | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005747-29 | Sponsor Protocol Number: BP20843 | Start Date*: 2007-03-14 | ||||||||||||||||
Sponsor Name:F. HOFFMANN-LA ROCHE LTD | ||||||||||||||||||
Full Title: Evaluation of the relationship between HDL quantity and HDL functionality in patients treated with HDL-C raising drugs | ||||||||||||||||||
Medical condition: Primary hypercholesterolemia or mixed dyslipidemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003406-10 | Sponsor Protocol Number: BC21144 | Start Date*: 2007-12-13 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A Phase IIb, Multi-Center, Double-Blind, Randomized, Placebo-Controlled Study, Evaluating the Safety, Tolerability and Efficacy of RO4607381 by Measuring Flow Mediated Dilatation in the Brachial Ar... | |||||||||||||
Medical condition: Patients with Coronary Heart Disease (CHD) or CHD Risk Equivalents | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DE (Completed) IT (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001491-11 | Sponsor Protocol Number: EV01 | Start Date*: 2020-07-24 | |||||||||||||||||||||
Sponsor Name:IRCCS SAN RAFFAELE PISANA GESTITO DA SAN RAFFAELE ROMA SRL | |||||||||||||||||||||||
Full Title: Phase IV study for efficacy and safety of Evolocumab added to Ezetimibe (Standard of Care) in high cardiovascular risk haemodialized statin intolerant patients with hypercholesterolemia. | |||||||||||||||||||||||
Medical condition: High cardiovascular risk haemodialized statin intolerant patients with hypercholesterolemia. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003014-22 | Sponsor Protocol Number: Thalamus_V3 | Start Date*: 2018-06-25 |
Sponsor Name:Medical University of Vienna | ||
Full Title: The role of leptin in regulating hepatic lipid metabolism in humans | ||
Medical condition: lipodystrophy patients, patients after liver transplantation and healthy controls | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003532-39 | Sponsor Protocol Number: SitaBAT01 | Start Date*: 2014-11-24 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of sitagliptin on brown adipose tissue and whole-body metabolism in overweight pre-diabetic men | ||
Medical condition: Obesity, dyslipidemia and impaired glucose tolerance | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001730-19 | Sponsor Protocol Number: v1-2 | Start Date*: 2022-02-24 |
Sponsor Name:Medical Univerity of Vienna | ||
Full Title: Hormones and Muscle – Unravelling the metabolic pathways of endocrine myopathies A translational magnetic resonance spectroscopy and imaging pilot study | ||
Medical condition: Hypothyroidism Hypoparathyroidism | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000831-34 | Sponsor Protocol Number: GoforGH | Start Date*: 2022-01-11 |
Sponsor Name:Medical University of Vienna | ||
Full Title: InvestiGating the rOle of Growth Hormone in hepatic lipid metabolism in humans | ||
Medical condition: Healthy subjects | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004846-25 | Sponsor Protocol Number: Pfizer-Prevenar13-2015 | Start Date*: 2016-07-15 |
Sponsor Name:Maastricht University | ||
Full Title: Immunization against oxLDL in patients with lysosomal lipid diseases and associated metabolic disorders | ||
Medical condition: Familial hypercholesterolemia Niemann-Pick disease type B (NPB) Niemann-Pick disease type C (NPC) Partial lipodystrophy in children and adults | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002221-31 | Sponsor Protocol Number: CCB-CRC-05-1 | Start Date*: 2005-08-11 |
Sponsor Name:Clinic for Nephrology | ||
Full Title: Efficacy of niacin on phosphatic metabolism in patients with renal insufficiency | ||
Medical condition: Exam the efficacy of niaspan in phosphate metabolism of patients with renal insufficiency, different exam for dialysis and predialysis patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000823-15 | Sponsor Protocol Number: DIASA3 | Start Date*: 2019-10-18 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Glucose metabolism in South Asian women with impaired glucose tolerance or impaired fasting glucose. DIAbetes in South Asians – DIASA 3 A 12-week intervention trial with oral antidiabetic medicati... | |||||||||||||
Medical condition: Pre-diabetes in women of South Asian ethnicity. Women of South Asian ethnicity with previous gestational diabetes, where pre-diabetes in the form of impaired glucose tolerance or impaired fasting ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000152-34 | Sponsor Protocol Number: 2012-000152-34 | Start Date*: 2012-02-09 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: evaluation of the effect of treatment with DPP-4 inhibitor on endothelial function versus sulphonylurea on markers of oxidative stress and inflammation and platelet function in patients with diabet... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001513-13 | Sponsor Protocol Number: LAL-CL04 | Start Date*: 2011-10-24 | |||||||||||||||||||||
Sponsor Name:Synageva Biopharma Corp. | |||||||||||||||||||||||
Full Title: AN OPEN LABEL MULTICENTER EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF SBC-102 IN ADULT SUBJECTS WITH LIVER DYSFUNCTION DUE TO LYSOSOMAL ACID LIPASE DEFICIENCY WH... | |||||||||||||||||||||||
Medical condition: Lysosomal Acid Lipase (LAL) Deficiency is a rare autosomal recessive lipid storage disorder that is caused by deficient activity or absence, of the lysosomal enzyme, LAL. It is an extremely rare di... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002418-12 | Sponsor Protocol Number: CFEM345D2407 | Start Date*: 2005-01-25 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open-label, randomized, multicenter safety study to evaluate the skeletal and lipid profile effects of letrozole and tamoxifen in postmenopausal women with resected, receptor positive early brea... | ||
Medical condition: Bone loss attributed to cessation of ovarian estrogen production is common in postmenopausal women. In postmenopausal women with breast cancer, treatment with an aromatase inhibitor may further red... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) GB (Completed) | ||
Trial results: View results |
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