- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Membrane Lipid.
Displaying page 1 of 1.
EudraCT Number: 2016-003902-14 | Sponsor Protocol Number: 16-118 | Start Date*: 2017-07-06 |
Sponsor Name:RWTH Aachen University, represented by the Clinical Trial Center (CTC-A) | ||
Full Title: Intravenous Fish Oil based Lipid Emulsion as Pharmaconutrient Strategy in High-Risk Cardiac Surgery Patients: a Phase II Dosing Study | ||
Medical condition: Given the recently meta-analyzed data from previous RCTs about fish oil , we hypothesize that the provision of intravenous (i.v.) FO (0.20 g/kg and 0.50 g/kg) to cardiac surgery patients may reduc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005274-30 | Sponsor Protocol Number: UCL_2011_DIDo | Start Date*: 2012-08-27 | |||||||||||
Sponsor Name:Université catholique de Louvain | |||||||||||||
Full Title: Efficacy and safety of a Double Icodextrin Dose in elderly incident CAPD patients on incremental Peritoneal Dialysis therapy: the DIDo study | |||||||||||||
Medical condition: Patients with chronic renal failure who are starting a Continuous Ambulatory Peritoneal Dialysis (CAPD) as first line dialyse. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020516-11 | Sponsor Protocol Number: CRCFC-DHA002 | Start Date*: 2010-09-16 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ISTITUTI OSPITALIERI DI VERONA | ||||||||||||||||||
Full Title: EXPERIMENTAL STUDY, RANDOMIZED, OPEN LABEL, TO EVALUATE THE EFFECT OF DOCOSAHEXAENOIC ACID (DHA) SUPPLEMENTATION VERSUS 5-METHYLTETHRAHYDROFOLATE + B12 VITAMIN AND DHA, IN CYSTIC FIBROSIS PATIENTS ... | ||||||||||||||||||
Medical condition: CYSTIC FIBROSIS AND PANCREATIC INSUFFICIENCY | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012185-32 | Sponsor Protocol Number: ML22413 | Start Date*: 2009-11-23 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Open label, multicentric phase IIIb study to evaluate the effect of tocilizumab in combination with DMARDs in the inhibition of progression of synovitis, bone marrow edema, and erosions evaluated b... | |||||||||||||
Medical condition: Moderate to severe active rheumatoid arthritis (RA), who are inadequate responders to DMARDs. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001235-30 | Sponsor Protocol Number: MSI-1256F-302 | Start Date*: 2005-10-26 |
Sponsor Name:Genaera Corporation | ||
Full Title: A Phase 3 Multicenter, Randomized, Double-Masked, Controlled Study of Squalamine Lactate (MSI-1256F) for Injection for the Treatment of Subfoveal Choroidal Neovascularization Associated with Age-Re... | ||
Medical condition: Subfoveal Choroidal Neovascularization Associated with Age-Related Macular Degeneration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010520-25 | Sponsor Protocol Number: AMR-01-01-0016 | Start Date*: 2009-12-08 | ||||||||||||||||
Sponsor Name:Amarin Pharma Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multi-Center, Placebo-Controlled, Randomized, Double-Blind, 12-Week Study With an Open-Label Extension to Evaluate the Efficacy and Safety of AMR101 in Patients With Fasting Triglycer... | ||||||||||||||||||
Medical condition: Hypertriglyceridemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) DK (Prematurely Ended) FI (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000942-39 | Sponsor Protocol Number: NL34476.068.11 | Start Date*: 2011-06-20 | ||||||||||||||||
Sponsor Name:CTMM, the Center for Translational Molecular Medicine | ||||||||||||||||||
Full Title: Effects of thyroid hormone treatment on mitochondrial function, ectopic fat accumulation, insulin sensitivity and brown adipose tissue in type 2 diabetes mellitus. | ||||||||||||||||||
Medical condition: This trial includes overweight patients with both hypothyroidism and type 2 diabetes. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004682-14 | Sponsor Protocol Number: OM-EPA-011 | Start Date*: 2014-04-15 | |||||||||||
Sponsor Name:Omthera Pharmaceuticals, Inc. | |||||||||||||
Full Title: A 12-Week, Randomized, Double-Blind, Olive Oil-Controlled Phase 3 Study to Assess the Efficacy and Safety of EPANOVAâ„¢ in Subjects With Severe Hypertriglyceridemia (EVOLVE II) | |||||||||||||
Medical condition: Severe hypertriglyceridemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000215-31 | Sponsor Protocol Number: S65796 | Start Date*: 2022-05-24 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: A monocentric academic trial comparing the diagnostic value of history taking and nasal lysine aspirin provocation test in the diagnosis of AERD in CRSwNP patients | |||||||||||||
Medical condition: Aspirin-Exacerbated Respiratory Disease (AERD) in patients with Chronic RhinoSinusitis with Nasal Polyps (CRSwNP) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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