- Trials with a EudraCT protocol (123)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
123 result(s) found for: Ethyl.
Displaying page 3 of 7.
| EudraCT Number: 2005-004473-14 | Sponsor Protocol Number: BAY 58-2667 / 11615 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Bayer HealthCare AG | ||
| Full Title: Proof of concept study to investigate the impact of BAY 58-2667 given intravenously in patients with acute decompensated chronic congestive heart failure | ||
| Medical condition: Critically ill patients, male and female, admitted to hospital with decompensated chronic congestive heart failure and clinical indication for parenteral pharmacotherapy with invasive hemodynamic m... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004969-41 | Sponsor Protocol Number: SPA-S-891/051 | Start Date*: 2006-02-14 | |||||||||||
| Sponsor Name:SOCIETA PRODOTTI ANTIBIOTICI | |||||||||||||
| Full Title: A double-blind, controlled vs placebo trial to evaluate the efficacy of EPA and DHA ethyl esters, in addition to usual antiarrhythmic therapy, in the manintenance of synus rythm in patients candida... | |||||||||||||
| Medical condition: Patients with persistent atrial fibrillation candidated to electrical cardioversion. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024547-32 | Sponsor Protocol Number: RBHP 2010 AZARNOUSCH | Start Date*: 2011-03-17 |
| Sponsor Name:CHU Clermont-Ferrand | ||
| Full Title: Effets potentiels d’une supplémentation en oméga 3 sur la membrane des cardiomyocytes de patients atteints d’athérosclérose coronaire ? | ||
| Medical condition: patients avec indication de chirurgie de revascularisation coronaire | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000163-25 | Sponsor Protocol Number: HE2006 | Start Date*: 2005-08-04 |
| Sponsor Name:Research and Enterprise, University of Birmingham | ||
| Full Title: Proteomics and Pharmacokinetics of Adriamycin Following Different Techniques for Chemoembolisation of Hepatocellular Carcinoma (PPATCH) Trial | ||
| Medical condition: Hepatocellular cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-006465-38 | Sponsor Protocol Number: 21EU-Fpf02 | Start Date*: 2022-06-06 | |||||||||||||||||||||
| Sponsor Name:IBSA Institut Biochimique S.A. | |||||||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Multi-Centre, Placebo-Controlled, Active Comparator Study to Evaluate the Efficacy and Safety of a diclofenac epolamine (DHEP) 2.6% medicated plaster in the treatment of... | |||||||||||||||||||||||
| Medical condition: Acute pain in mild/moderate ankle sprains | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: PL (Completed) CZ (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-000169-19 | Sponsor Protocol Number: | Start Date*: 2019-09-03 | ||||||||||||||||
| Sponsor Name:Queen Mary University London | ||||||||||||||||||
| Full Title: Clinical trial to determine the effect of Famciclovir on Epstein-Barr virus activity as measured by EBV shedding in saliva of patients with Multiple Sclerosis. | ||||||||||||||||||
| Medical condition: Epstein Barr virus infection in people with multiple sclerosis. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002692-34 | Sponsor Protocol Number: MitoFibrateCT1-2012 | Start Date*: 2013-06-26 |
| Sponsor Name:Univ.-Klinik für Kinder- und Jugendheilkunde | ||
| Full Title: Clinical study for the assessment of safety and efficacy of Bezafibrate as a drug therapy for patients with mitochondrial myopathies | ||
| Medical condition: mitochondrial disorder | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000364-21 | Sponsor Protocol Number: PI1102031 | Start Date*: 2012-11-13 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomédica | |||||||||||||
| Full Title: FDDNP-PET FOR IN VIVO DIAGNOSIS OF TAUOPATHY IN UNCLASSIFIABLE PARKINSONISM | |||||||||||||
| Medical condition: Atypical Parkinsonism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000330-50 | Sponsor Protocol Number: EC07/90285 | Start Date*: 2008-10-27 | |||||||||||
| Sponsor Name:Organisation name was not entered | |||||||||||||
| Full Title: EFECTO DE SUPLEMENTACIÓN NUTRICIONAL ENRIQUECIDA CON ÁCIDOS GRASOS OMEGA-3 EN EL ESTRÉS OXIDATIVO Y METABOLISMO LIPÍDICO DE PACIENTES CON PROCESOS ONCOLÓGICOS DEL ÁREA OTORRINOLARINGOLÓGICA (ORL) ... | |||||||||||||
| Medical condition: Determinar las modificaciones inducidas por la suplementación especifica de ácidos grasos omega3 en el estrés oxidativo y estado inflamatorio en pacientes oncológicos sometidos a tratamiento radiot... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001531-32 | Sponsor Protocol Number: Obadiah-2 | Start Date*: 2019-12-20 | |||||||||||
| Sponsor Name:Imperial College Healthcare NHS Trust | |||||||||||||
| Full Title: OBADIAH-2: A randomised, double-blind, placebo-controlled trial of two doses of obeticholic acid and placebo in patients with primary bile acid diarrhoea | |||||||||||||
| Medical condition: Bile acid diarrhoea (also known as bile acid malabsorption) | |||||||||||||
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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: 2016-000628-24 | Sponsor Protocol Number: MO16/053 | Start Date*: 2018-01-12 | |||||||||||
| Sponsor Name:University of Leeds | |||||||||||||
| Full Title: A randomised placebo-controlled phase III trial of the effect of the omega-3 fatty acid eicosapentaenoic acid (EPA) on colorectal cancer recurrence and survival after surgery for resectable liver m... | |||||||||||||
| Medical condition: Colorectal cancer liver metastases | |||||||||||||
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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: 2011-001290-78 | Sponsor Protocol Number: 007697 | Start Date*: 2012-01-17 |
| Sponsor Name:Barts Health NHS Trust | ||
| Full Title: Diagnostic accuracy of MRI, diffusion-weighted MRI, FDG-PET/CT and Fluoro-ethyl-choline PET/CT in the detection of lymph node metastases in surgically staged endometrial and cervical carcinoma | ||
| Medical condition: Endometrial and Cervical Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000748-24 | Sponsor Protocol Number: TF-TF0023-201 | Start Date*: 2022-08-26 | |||||||||||
| Sponsor Name:Techfields Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-blind (Within Dose), Placebo-controlled, Parallel-group, and Dose-range-finding Study to Evaluate the Efficacy and Safety of TF0023 Versus Placebo in Trea... | |||||||||||||
| Medical condition: COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003380-26 | Sponsor Protocol Number: TCP-304 | Start Date*: 2021-01-05 | |||||||||||
| Sponsor Name:Ascendis Pharma Bone Diseases A/S | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial, with an Open-Label Extension, Investigating the Safety, Tolerability and Efficacy of TransCon PTH Admini... | |||||||||||||
| Medical condition: Hypoparathyroidism in Adults | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) NO (Completed) FR (Completed) DE (Completed) HU (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004016-11 | Sponsor Protocol Number: 2305 | Start Date*: 2016-06-30 | ||||||||||||||||
| Sponsor Name:University of Bristol | ||||||||||||||||||
| Full Title: What is the clinical and cost effectiveness of benzocaine/phenazone ear drops for reducing antibiotic consumption and ear pain in children aged between 6 months and 10 years presenting to primary c... | ||||||||||||||||||
| Medical condition: Acute otitis media | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-000883-16 | Sponsor Protocol Number: 200699 | Start Date*: 2014-07-03 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Devlopment Ltd | ||||||||||||||||||
| Full Title: A Clinical Study to Evaluate Four Doses of Umeclidinium Bromide in Combination with Fluticasone Furoate in COPD Subjects with an Asthmatic Component | ||||||||||||||||||
| Medical condition: COPD Subjects with an Asthmatic Component | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) RO (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-004815-33 | Sponsor Protocol Number: TransCon_PTH_TCP-201 | Start Date*: 2019-09-27 | |||||||||||
| Sponsor Name:Ascendis Pharma Bone Diseases A/S | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial with an Open-Label Extension, Investigating the Safety, Tolerability and Efficacy of TransCon PTH Administ... | |||||||||||||
| Medical condition: Hypoparathyroidism (HP) in Adults | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Trial now transitioned) DE (Trial now transitioned) DK (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003548-22 | Sponsor Protocol Number: LAEBBA0005 | Start Date*: 2014-03-03 |
| Sponsor Name:Johnson & Johnson Consumer & Personal Products Worldwide, Division of Johnson & Johnson Consumer Companies, Inc | ||
| Full Title: Four Week Clinical Efficacy of An Ethyl Lauroyl Arginate HCL (LAE) Mouth Rinse: Effect on Gingivitis | ||
| Medical condition: Gingivitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004286-32 | Sponsor Protocol Number: ikfe-Vilda-001 | Start Date*: 2011-11-09 | ||||||||||||||||
| Sponsor Name:ikfe GmbH | ||||||||||||||||||
| Full Title: Effect of Adding Vildagliptin on Beta Cell Function and Cardiovascular Risk Markers in Patients with moderate Metabolic Control during Metformin Monotherapy | ||||||||||||||||||
| Medical condition: Diabetes mellitus Type 2 | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-001856-19 | Sponsor Protocol Number: MRVT-920101-OPH005 | Start Date*: 2005-10-24 |
| Sponsor Name:Miravant Pharmaceuticals, Inc. | ||
| Full Title: A Phase III Randomized, Multicenter, Multinational, Double-Masked, Placebo-Controlled Study of Photrex™ (Rostaporfin) Photodynamic Therapy in the Treatment of Classic and Occult Subfoveal Choroidal... | ||
| Medical condition: classic and occult subfoveal choroidal neovascularization (CNV) associated with age-related macular degeneration (AMD). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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