- Trials with a EudraCT protocol (3,941)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
3,941 result(s) found for: Liver diseases.
Displaying page 1 of 198.
EudraCT Number: 2012-000834-21 | Sponsor Protocol Number: POCHER-2/AIRC11770 | Start Date*: 2012-04-01 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: Molecular Biomarkers for Colorectal Liver Metastases Resectability after Chemotherapy with Cetuximab | |||||||||||||
Medical condition: PATIENTS WITH LIVER COLORECTAL METASTASES NOT CANDIDATED TO SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001222-83 | Sponsor Protocol Number: HHSC/001 | Start Date*: 2005-12-09 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A phase I/II safety and tolerability dose escalation study following the autologous infusion of expanded adult haemopoietic stem cells to patients with liver insufficiency | ||||||||||||||||||
Medical condition: Chronic liver insufficiency | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005454-35 | Sponsor Protocol Number: MG001 | Start Date*: 2013-03-13 | |||||||||||
Sponsor Name:Hanna Pitkänen | |||||||||||||
Full Title: Can magnesium enhance blood coagulation amongst patients with alcohol induced liver cirrhosis? | |||||||||||||
Medical condition: Liver transplant candidates with alcohol induced liver cirrhosis and hypomagnesemia (P-Mg under 0,71 or magnesium substitution at least 750 mg/day) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006227-38 | Sponsor Protocol Number: 11.017 | Start Date*: 2012-05-01 | ||||||||||||||||
Sponsor Name:Ove B. Schaffalitzky de Muckadell | ||||||||||||||||||
Full Title: “Assessment of fibrotic liver disease in a medical admission ward and intervention with losartan as antifibrotic therapy in patients with alcoholic liverdisease” | ||||||||||||||||||
Medical condition: Fibrotic alcoholic liver disease is in early stages often completely asymptomatic. Fully developed cirrhosis affect a wide range of physiological conditions. Eksamples are portal hypertension and f... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006023-33 | Sponsor Protocol Number: SIMFIB | Start Date*: 2021-10-26 | ||||||||||||||||
Sponsor Name:Institut d’Investigacions Biomèdiques August Pi i Sunyer | ||||||||||||||||||
Full Title: Efficacy of simvastatin reducing liver fibrosis in patients with advanced fibrosis due to alcohol: a randomized, double-blind, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: reduction of liver fibrosis in patients with advanced fibrosis due to alcohol | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001449-42 | Sponsor Protocol Number: VITDCirrhosis2012 | Start Date*: 2014-10-03 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Kl. Abt. f. Endokrinoloie u. Stoffwechsel & Kl. Abt. f. Gastroenterologie u. Hepatologie | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled trial to evaluate vitamin D supplementation on serum 25 hydroxy- vitamin D level in cirrhotic patients | |||||||||||||
Medical condition: decompensated and compensated liver cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000983-27 | Sponsor Protocol Number: CLCZ696B2203 | Start Date*: 2012-09-07 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single-dose, open-label parallel-group study to assess the pharmacokinetics of LCZ696 in subjects with hepatic impairment compared to matched healthy subjects | |||||||||||||
Medical condition: Mild and moderate hepatic impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005628-13 | Sponsor Protocol Number: IRRB/34/12 | Start Date*: 2012-12-19 | ||||||||||||||||||||||||||
Sponsor Name:ISTITUTO MEDITERRANEO PER I TRAPIANTI E TERAPIE AD ALTA SPECIALIZZAZIONE | ||||||||||||||||||||||||||||
Full Title: Transplantation of Human Fetal Liver Cells for the Treatment of Patients with Decompensated Liver Cirrhosis | ||||||||||||||||||||||||||||
Medical condition: liver cirrhosis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002856-34 | Sponsor Protocol Number: LTx18-01 | Start Date*: 2019-03-01 | |||||||||||
Sponsor Name:Foundation for Liver research | |||||||||||||
Full Title: Modifying tacrolimus related toxicity after liver transplantation. A randomized controlled trial comparing Envarsus® and Advagraf® in de novo liver transplant recipients. | |||||||||||||
Medical condition: liver transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000270-28 | Sponsor Protocol Number: NL75171.058.20 | Start Date*: 2022-06-30 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Selective Indocyanine Green Injection of a Segmental Hepatic Artery Followed by Near-Infrared Fluorescence Guided Anatomical Liver Resection: A Feasibility Study | ||
Medical condition: Hepatocellular carcinoma, hepatic adenoma, intrahepatic cholangiocarcinoma, colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
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: 2015-000963-15 | Sponsor Protocol Number: MATCH0.1 | Start Date*: 2016-01-19 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: MAcrophage Therapy for Liver Cirrhosis (MATCH) | |||||||||||||
Medical condition: Liver Cirrhosis | |||||||||||||
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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: 2012-001239-30 | Sponsor Protocol Number: CIR976101 | Start Date*: 2012-05-22 | |||||||||||
Sponsor Name:Foundation for Liver Research | |||||||||||||
Full Title: THE EFFECTS OF RECOMBINANT HUMAN INSULIN-LIKE GROWTH FACTOR-1 ON THE NUTRITIONAL STATUS IN PATIENTS WITH LIVER CIRRHOSIS: A PILOT-STUDY. | |||||||||||||
Medical condition: Liver cirrhosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001806-40 | Sponsor Protocol Number: STATLiver2019 | Start Date*: 2019-09-03 | |||||||||||
Sponsor Name:Afsnit 360, Gastroenheden | |||||||||||||
Full Title: Statins for prevention of disease progression and hospitalization in Liver Cirrhosis: A multi-center, randomized, double blind, placebo-controlled trial. The STATLiver Trial. | |||||||||||||
Medical condition: Cirrhosis of the liver | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002984-24 | Sponsor Protocol Number: PHS-Px-104-II-01 | Start Date*: 2013-10-07 | |||||||||||
Sponsor Name:Phenex Pharmaceuticals AG | |||||||||||||
Full Title: A Safety Pilot Study of Px-104 in non alcoholic fatty liver disease (NAFLD) patients | |||||||||||||
Medical condition: Non-alcoholic fatty liver disease (NAFLD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016761-29 | Sponsor Protocol Number: HE2013 | Start Date*: 2010-05-14 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: A 48-WEEK PHASE II, RANDOMISED, DOUBLE BLINDED PLACEBO CONTROLLED, PARALLEL-GROUP, MULTI-CENTRE TRIAL ON LIRAGLUTIDE’S SAFETY, EFFICACY AND ACTION ON LIVER HISTOLOGY AND METABOLISM IN OVERWEIGHT PA... | ||||||||||||||||||
Medical condition: Non-alcoholic steatohepatits (NASH) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003561-15 | Sponsor Protocol Number: MYSTEP1 | Start Date*: 2016-08-30 | |||||||||||
Sponsor Name:University Hospital of Tuebingen | |||||||||||||
Full Title: Safety and Tolerance of Immunomodulating Therapy with Donor-specific Mesenchymal Stem Cells in Pediatric Living-Donor Liver Transplantation | |||||||||||||
Medical condition: Side effects of life-long immunosuppressive medication account for major morbidity after pediatric liver transplantation and impair quality of life. In-vivo and in-vitro studies have shown that MSC... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007177-20 | Sponsor Protocol Number: Sirolimus_Liver_Tolerance | Start Date*: 2009-09-07 | |||||||||||
Sponsor Name:Hospital Clinic Barcelona | |||||||||||||
Full Title: EFECTO DEL SIROLIMUS SOBRE LOS BIOMARCADORES RELACIONADOS CON LA TOLERANCIA EN RECEPTORES DE TRASPLANTE HEPÁTICO ESTABLES | |||||||||||||
Medical condition: Stable liver transplant recipients identified as non-tolerant (i.e. requiring indefinite immunosuppressive therapy) on the basis of peripheral blood transcriptional biomarkers. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003349-41 | Sponsor Protocol Number: ERASMECMI | Start Date*: 2013-10-03 | |||||||||||
Sponsor Name:Erasme hospital | |||||||||||||
Full Title: what are the optimal doses of cefuroxime for cirrhotic patients? | |||||||||||||
Medical condition: Cirrhotic patients with infection requiring treatment with cefuroxime | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005453-13 | Sponsor Protocol Number: EGRADICATE | Start Date*: 2016-08-03 | ||||||||||||||||
Sponsor Name:Fundació clínic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: PILOT STUDY TO EVALUATE THE EFFICACY AND TOLERABILITY OF GRAZOPREVIR + ELBASVIR FOR 12 OR 16 WEEKS IN LIVER TRANSPLANT RECIPIENTS | ||||||||||||||||||
Medical condition: HCV infection and liver trasplant | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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