- Trials with a EudraCT protocol (396)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
396 result(s) found for: Emulsion.
Displaying page 1 of 20.
EudraCT Number: 2022-000660-22 | Sponsor Protocol Number: Benzylbenzoat-Permethrin-5020 | Start Date*: 2022-06-14 |
Sponsor Name:Landeskrankenhaus Salzburg | ||
Full Title: Investigation to assess the efficacy of topical benzyl benzoate 10/25% emulsion versus permethrin 5% creme for scabies treatment | ||
Medical condition: Scabies | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003255-15 | Sponsor Protocol Number: Benzylbenzoat-Ivermectin-5020 | Start Date*: 2020-12-17 |
Sponsor Name:Landeskrankenhaus Salzburg | ||
Full Title: Investigation to assess the efficacy of benzyl benzoate 10/25% emulsion versus oral ivermectin for scabies treatment | ||
Medical condition: Scabies | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002715-10 | Sponsor Protocol Number: FAR-NP-2018-01 | Start Date*: 2019-02-08 |
Sponsor Name:Elisabet Leiva Badosa. Phamacy Department. Hospital Universitari de Bellvitge | ||
Full Title: RANDOMIZED, DOUBLE-BLIND, PILOT CLINICAL TRIAL TO COMPARE THE EFFICACY AND SAFETY OF FISH OIL-BASED INTRAVENOUS LIPID EMULSIONS IN HOSPITALIZED ADULT PATIENTS TREATED WITH TOTAL PARENTERAL NUTRITIO... | ||
Medical condition: Hypertriglyceridemia is a frequent metabolic complication associated with the administration of lipidic emulsion in total parenteral nutrition. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000406-51 | Sponsor Protocol Number: EMD20001 | Start Date*: 2004-09-16 |
Sponsor Name:GlaxoSmithKline | ||
Full Title: A Prospective, Randomized, Double-blind, Placebo Controlled, Dose Ranging, Multi-Center Study of the Safety and Efficacy of Three Days Continuous Intravenous Infusion of GR270773 in the Treatment o... | ||
Medical condition: Suspected or Confirmed Gram-negative Severe Sepsis in Adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) ES (Completed) CZ (Completed) LV (Completed) AT (Completed) HU (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001653-28 | Sponsor Protocol Number: 03/314 | Start Date*: Information not available in EudraCT |
Sponsor Name:The Leeds teaching Hospitals NHS trust | ||
Full Title: A comparison of the effects on prostaglandin synthesis and cytokine production of an olive-oil based lipid emulsion (Clinoloeic) with a soya based emulsion (Intralipid) in newborn infnats receiving... | ||
Medical condition: Prematurity Parenteral nutrition | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005456-33 | Sponsor Protocol Number: | Start Date*: 2012-01-26 |
Sponsor Name:Med. Univ. Wien, Universitätsklinik für Kinder- und Jugendheilkunde | ||
Full Title: PREVENTING CHOLESTASIS IN PREMATURE INFANTS USING SMOFLIPID | ||
Medical condition: • To compare a mixed parenteral lipid emulsion containing fish oil (SMOFlipid®) with a soybean oil based lipid emulsion (Intralipid®) for its effect on the occurrence of parenteral nutrition associ... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001743-31 | Sponsor Protocol Number: 18-03/MPA-M | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Methylprednisolone Aceponate 0.1% Cutaneous emulsion (Test) vs. Advantan Milk 0.1% Cutaneous emulsion (Reference) vs. Vehicl... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002351-34 | Sponsor Protocol Number: V1.0 | Start Date*: 2013-02-21 |
Sponsor Name:Medizinische Universitaet Wien, Univ.Klinik f.Innere Medizin III, Abteilung fuer Gastroenterologie und Hepatologie | ||
Full Title: Effects of oral and intravenous lipid load on Hepatitis C virus concentrations in serum and lipoprotein subfractions | ||
Medical condition: chronic hepatitis C | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001126-90 | Sponsor Protocol Number: H 1000 2925-06/08 | Start Date*: 2006-07-06 | |||||||||||
Sponsor Name:Hermal Kurt Herrmann GmbH & Co. OHG | |||||||||||||
Full Title: Evaluation of safety and efficacy of Curatoderm® Emulsion in the treatment of patients with mild to moderate plaque psoriasis | |||||||||||||
Medical condition: Patients with mild to moderate plaque type Psoriasis vulgaris. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002425-31 | Sponsor Protocol Number: 05-SMOF-006 | Start Date*: 2007-03-19 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: A double-blind, randomised study comparing the safety and tolerance of SMOFlipid 20% and Intralipid 20% in long-term treatment with parenteral nutrition | |||||||||||||
Medical condition: Supply of energy, essential fatty acids and omega-3 fatty acids to adults, as part of a parenteral nutrition regimen, when oral or enteral nutrition is impossible, insufficient or contra-indicated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000849-23 | Sponsor Protocol Number: HC-G-H-1403 | Start Date*: 2017-08-21 | |||||||||||
Sponsor Name:B. Braun Melsungen AG | |||||||||||||
Full Title: A RANDOMIZED, CONTROLLED, DOUBLE-BLIND, MULTICENTER CLINICAL TRIAL ON HOME PARENTERAL NUTRITION USING AN OMEGA-3 FATTY ACID ENRICHED MCT/LCT LIPID EMULSION | |||||||||||||
Medical condition: Chronic intestinal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003571-39 | Sponsor Protocol Number: HC-G-H-0705 | Start Date*: 2008-04-23 |
Sponsor Name:B. Braun Melsungen AG | ||
Full Title: Prospective, monocentric, controlled, randomized, double-blind study to compare two different propofol emulsions regarding tolerability and injection pain during the induction of anesthesia in adults | ||
Medical condition: reduction of injection pain during induction of anaesthesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001341-41 | Sponsor Protocol Number: EKTKet01 | Start Date*: 2012-11-13 |
Sponsor Name:Universitätsklinik für Psychiatrie und Psychotherapie I | ||
Full Title: Propofol vs. Ketamin | ||
Medical condition: major depression, bipolar disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000552-27 | Sponsor Protocol Number: ACO2008-CT-01 | Start Date*: 2008-06-11 |
Sponsor Name:ACO HUD NORDIC AB | ||
Full Title: Effect of moisturizing creams on skin barrier function and prevention of Malassezia recurrence in patients with atopic eczema | ||
Medical condition: Dry skin barrier disorders such as atopic eczema and ichtyosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018660-16 | Sponsor Protocol Number: SAP version1 01/01/2010 | Start Date*: 2010-04-22 |
Sponsor Name:University Hospitals of leicester NHS Trust | ||
Full Title: Randomised controlled trial on the effects of parenteral fish oil emulsion in patients with severe acute pancreatitis | ||
Medical condition: Acute Pancreatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016880-13 | Sponsor Protocol Number: ITU version1 19/10/2009 | Start Date*: 2011-03-11 |
Sponsor Name:UNIVERSITY HOSPITALS OF LEICESTER NHS TRUST | ||
Full Title: RANDOMIZED CONTROLLED TRIAL OF THE EFFECTS OF PARENTERAL FISH OIL EMULSION IN CRITICALLY ILL SEPTIC PATIENTS IN THE INTENSIVE CARE UNIT | ||
Medical condition: Sepsis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002206-10 | Sponsor Protocol Number: APHP190891 | Start Date*: 2020-07-07 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: A prospective study of the safety and efficacy of the use of a Lipiodol Emulsion for the embolization of inflammatory hypervascularizations observed in patients with articular or abarticular pain i... | ||
Medical condition: Adult patients with articular or abarticular intractable pain in the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003397-82 | Sponsor Protocol Number: HC-G-H-0813 | Start Date*: 2012-12-12 | |||||||||||
Sponsor Name:B. Braun Melsungen AG | |||||||||||||
Full Title: Prospective, randomized, controlled, double-blind, parallel-group, mono-centre, explorative Phase IV trial on the efficacy and safety of a fish oil containing lipid emulsion versus a standard soybe... | |||||||||||||
Medical condition: Acute Lung Injury as a result of proven pneumonia (x-ray) or witnessed aspiration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002380-90 | Sponsor Protocol Number: IVN3DIALYSE | Start Date*: 2005-09-26 |
Sponsor Name:Nyremedicinsk afdeling, Aalborg Sygehus | ||
Full Title: Effekten af intravenøs infusion af n-3 polyumættede fedtsyrer på risikomarkører for pludselig hjertedød hos hæmodialysepatienter | ||
Medical condition: Chronic renal failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001212-30 | Sponsor Protocol Number: GW/MB/42964 | Start Date*: 2013-07-04 |
Sponsor Name: | ||
Full Title: Modulation of immune function by parenteral fish oil in patients with Crohn’s disease and high inherent Tumor Necrosis Factor-alfa production, a randomized, single blinded, cross-over study | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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