- Trials with a EudraCT protocol (147)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
147 result(s) found for: Fatty liver disease.
Displaying page 1 of 8.
EudraCT Number: 2014-003422-41 | Sponsor Protocol Number: Rifa-Stea | Start Date*: 2014-10-13 | |||||||||||
Sponsor Name:Oulu University Hospital, Department of Internal Medicine | |||||||||||||
Full Title: The effects of PXR activation on hepatic fat content | |||||||||||||
Medical condition: Healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008275-34 | Sponsor Protocol Number: Edi-Omeg3-08001 | Start Date*: 2009-08-20 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: The Effect of Omega-3 Fatty Acids on Non-Alcoholic Fatty Liver Disease | |||||||||||||
Medical condition: Non-alcoholic fatty liver disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015703-13 | Sponsor Protocol Number: InReTel | Start Date*: 2009-12-11 | ||||||||||||||||||||||||||
Sponsor Name:Klinik für Innere Medizin II der Klinikum Chemnitz gGmbH | ||||||||||||||||||||||||||||
Full Title: The influence of Telmisartan on insulin resistance and fatty liver in patients suffer from hypertension | ||||||||||||||||||||||||||||
Medical condition: Influence of Telmisartan on insulin resistance, hypertension, non-alcoholic fatty liver | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003766-26 | Sponsor Protocol Number: 25-12-59 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Southampton University Hospitals NHS Trust | |||||||||||||
Full Title: The effects of purified n-3 fatty acids on serum biomarkers and cardiovascular risk markers in a randomized placebo controlled trial in patients with non alcoholic fatty liver disease | |||||||||||||
Medical condition: Non alcoholic fatty liver disease (NAFLD). This fatty liver disease may progress to a chronic condition that sometimes deteriorates further to cirrhosis and even liver carcinoma. To date there is n... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006677-26 | Sponsor Protocol Number: 68797373 | Start Date*: 2022-06-22 | ||||||||||||||||
Sponsor Name:Maastricht University | ||||||||||||||||||
Full Title: Metabolic effects of ketohexokinase inhibition in individuals with non-alcoholic fatty liver disease | ||||||||||||||||||
Medical condition: Healthy volunteers (non-alcoholic fatty liver disease) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005531-28 | Sponsor Protocol Number: Urso in Obese | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name:Hanns-Ulrich Marschall | |||||||||||||
Full Title: Ursodeoxycholic Acid in Morbidly Obese Patients Before Bariatric Surgery | |||||||||||||
Medical condition: Patients with morbid obesity (MB) are investigated. MB is very frequently (90%) associated with non-alcoholic fatty liver disease (NAFLD) comprising a spectrum reaching from steatosis (NAFL) over s... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003168-37 | Sponsor Protocol Number: CAIN457ADE15 | Start Date*: 2019-12-04 | ||||||||||||||||
Sponsor Name:Novartis Pharma GmbH | ||||||||||||||||||
Full Title: A randomized, double-blind, multicenter, 24-week study of subcutaneous secukinumab to assess anti-interleukin-17A treatment in plaque psoriasis patients with coexisting non-alcoholic fatty liver di... | ||||||||||||||||||
Medical condition: plaque psoriasis with coexisting non-alcoholic fatty liver disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021515-17 | Sponsor Protocol Number: N/A | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: RiFL: Rifaxamin in Fatty Liver Disease. Does Modulation of Gut Microbiota Reduce Hepatic Inflammation in Non-Alcoholic Steatohepatitis (NASH)? | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000813-37 | Sponsor Protocol Number: OCABSGS | Start Date*: 2012-05-16 | |||||||||||
Sponsor Name:Sahlgrenska Academy | |||||||||||||
Full Title: Effects of obeticholic acid on hepatic fatty acid/triglyceride metabolism and hepatobiliary detoxification/elimination in morbidly obese and gallstone patients. | |||||||||||||
Medical condition: Fatty liver disease, morbid obesity, gallstone disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004605-38 | Sponsor Protocol Number: NUC-4/NAS | Start Date*: 2015-02-11 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase II dose-finding study comparing different doses of norursodeoxycholic acid capsules with placebo in the treatment of non-alcoholic fatty liver di... | |||||||||||||
Medical condition: Non-alcoholic fatty liver disease (NAFLD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001975-36 | Sponsor Protocol Number: 201200197536 | Start Date*: 2012-05-24 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Evaluation on the efficacy of docosahexaenoic acid for the treatment of nonalcoholic fatty liver disease in children | |||||||||||||
Medical condition: Nonalcoholic steatohepatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015166-62 | Sponsor Protocol Number: EME-08/43/15 | Start Date*: 2010-11-16 | |||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial of Losartan as an anti-fibrotic agent in non-alcoholic steatohepatitis. | |||||||||||||
Medical condition: Fibrosis in patients with non-alcoholic steatohepatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000152-19 | Sponsor Protocol Number: 1 | Start Date*: 2022-02-24 |
Sponsor Name:Consorcio Centro de Investigación Biomédica en Red, M.P. (CIBER) | ||
Full Title: Control strategies and pharmacogenetic study for the personalized treatment of fatty liver associated with metabolic dysfunction in patients with prediabetes. | ||
Medical condition: Metabolic Associated Fatty Liver Disease with prediabetes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004141-24 | Sponsor Protocol Number: 228763 | Start Date*: 2018-01-26 | ||||||||||||||||
Sponsor Name:Brighton and Sussex University Hospitals NHS Trus | ||||||||||||||||||
Full Title: A phase IV, open-label pilot study investigating non-invasive markers of hepatic fibrosis in people living with HIV-1 and non-alcoholic fatty liver disease randomised to receiving optimised backgro... | ||||||||||||||||||
Medical condition: Non-alcoholic fatty liver disease in people living with well-controlled HIV-1 infection | ||||||||||||||||||
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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: 2014-003164-21 | Sponsor Protocol Number: 652-2-203 | Start Date*: 2015-01-05 | |||||||||||
Sponsor Name:Tobira Therapeutics, Inc., a subsidiary of Allergan plc | |||||||||||||
Full Title: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects with Liver Fibrosis | |||||||||||||
Medical condition: Nonalcoholic Steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) IT (Completed) DE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021368-13 | Sponsor Protocol Number: MTQ-LD-001 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:Antipodean Pharmaceuticals | |||||||||||||
Full Title: A Double-blind Randomised Placebo-controlled Multicentre Study of 40mg MitoQ and Placebo for the Treatment of Participants with Raised Liver Enzymes due to Non-Alcoholic Fatty Liver Disease (NAFLD) | |||||||||||||
Medical condition: Raised Liver Enzymes due to Non-Alcoholic Fatty Liver Disease (NAFLD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002253-29 | Sponsor Protocol Number: CEC-11/NAS | Start Date*: 2022-03-08 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase II dose-finding study comparing different doses of ZED1227 capsules with placebo in the treatment of non-alcoholic fatty liver disease (NAFLD) wi... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005187-63 | Sponsor Protocol Number: FM101-CTP2-001 | Start Date*: 2021-04-14 | ||||||||||||||||
Sponsor Name:Future Medicine Co., Ltd. | ||||||||||||||||||
Full Title: A Randomized Phase 2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of FM101 in Adults with Nonalcoholic Fatty Liver Disease (NAFLD) or Nonalcoholic Steatohepatitis (NASH) | ||||||||||||||||||
Medical condition: Nonalcoholic Fatty Liver Disease (NAFLD) or Nonalcoholic Steatohepatitis (NASH) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017080-41 | Sponsor Protocol Number: GWMD09112 | Start Date*: 2010-04-19 | |||||||||||
Sponsor Name:GW Pharma Ltd. | |||||||||||||
Full Title: A randomised, partially-blind, placebo-controlled, pilot, dose-ranging study to assess the effect of cannabidiol (CBD) on liver fat levels in subjects with fatty liver disease. | |||||||||||||
Medical condition: Subjects with fatty liver disease (≥ 5% liver fat levels). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004402-55 | Sponsor Protocol Number: 6344-001A | Start Date*: 2020-11-09 | |||||||||||
Sponsor Name:Baxter Healthcare Corporation | |||||||||||||
Full Title: A Randomized, Double-Blind, Controlled, Clinical Trial to Evaluate the Risk of Developing Essential Fatty Acid Deficiency in Pediatric Patients, Including Neonates, Receiving Either Clinolipid (lip... | |||||||||||||
Medical condition: Essential Fatty Acid Deficiency (EFAD) | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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