- Trials with a EudraCT protocol (121)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
121 result(s) found for: Hepatic encephalopathy.
Displaying page 3 of 7.
EudraCT Number: 2012-002120-33 | Sponsor Protocol Number: HLSCS01-11 | Start Date*: 2013-12-06 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | ||||||||||||||||||||||||||||
Full Title: Human Liver Stem Cells (HLSCs) in patients suffering from liver-based inborn metabolic diseases causing life-threatening neonatal onset of hyperammonemic encephalopathy | ||||||||||||||||||||||||||||
Medical condition: neonatal hyperammonemic encephalopathy associated with inborn liver metabolic diseases | ||||||||||||||||||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005523-27 | Sponsor Protocol Number: CIRROXABAN | Start Date*: 2015-07-30 |
Sponsor Name:INSTITUTO DE INVESTIGACIONES BIOMEDICAS AUGUST PI I SUNYER (IDIBAPS) | ||
Full Title: Multicenter prospective randomized trial of the effect of rivaroxaban on survival and development of complications of portal hypertension in patients with cirrhosis | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006042-33 | Sponsor Protocol Number: KAMON2 | Start Date*: 2007-02-01 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: A pilot, open label, multicenter, randomized clinical trial on Lopinavir/Ritonavir-monotherapy vs Lopinavir/Ritonavir plus selected Nucs, in HIV/HCV coinfected patients with chronic hepatitis C or... | |||||||||||||
Medical condition: patients affected by HIV and chronic HCV or compensated cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005996-17 | Sponsor Protocol Number: KAMON1 | Start Date*: 2007-02-02 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: A pilot, open label, multicenter, randomized clinical trial on Lopinavir/ritonavir-monotherapy vs Lopinavir/ritonavir plus selected Nucs, in HIV/HCV ARV-naive coinfected patients with chronic hepat... | |||||||||||||
Medical condition: PATIENTS AFFECTED BY HIV/HCV NAIVES FROM THERAPIES | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001698-25 | Sponsor Protocol Number: LIVERHOPE_EFFICACY | Start Date*: 2018-07-24 | |||||||||||
Sponsor Name:IDIBAPS | |||||||||||||
Full Title: Efficacy of the combination of simvastatin plus rifaximin in patients with decompensated cirrhosis to prevent ACLF development: a multicenter, double-blind, placebo controlled randomized clinical t... | |||||||||||||
Medical condition: Patients with decompensated cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) FR (Completed) GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004944-23 | Sponsor Protocol Number: WFTL001 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:Charité Universitätsmedizin | |||||||||||||
Full Title: | |||||||||||||
Medical condition: graft function adapted tacrolimus therapy after liver transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001787-10 | Sponsor Protocol Number: IG1407 | Start Date*: 2019-01-12 | |||||||||||
Sponsor Name:Instituto Grifols S.A. | |||||||||||||
Full Title: Effects of Plasma Exchange with Human Serum Albumin 5% (PE-A 5%) on Short-term Survival in Subjects with "Acute-On-Chronic Liver Failure" (ACLF) at High Risk of Hospital Mortality | |||||||||||||
Medical condition: Subjects with cirrhosis with ACLF-1b, ACLF-2, or ACLF-3a detected either at admission or during hospitalization | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) PT (Completed) DE (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) DK (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003724-79 | Sponsor Protocol Number: 17SM4152 | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: IL-1 Signal Inhibition in Alcoholic Hepatitis (Isaiah) | |||||||||||||
Medical condition: Alcoholic Hepatitis | |||||||||||||
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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: 2017-003629-13 | Sponsor Protocol Number: PROFIT | Start Date*: 2018-01-31 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: A Prospective, randomised placebo controlled feasibility trial of Faecal Microbiotica Transplantation in cirrhosis | |||||||||||||
Medical condition: Cirrhosis of the liver | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010760-42 | Sponsor Protocol Number: 4SC-201-1-2009 | Start Date*: 2009-06-19 | |||||||||||
Sponsor Name:4SC AG | |||||||||||||
Full Title: A proof-of-concept Phase II study to evaluate efficacy, safety and pharmacokinetics of 4SC-201 and the treatment combination of Sorafenib plus 4SC-201 in patients with hepatocellular carcinoma exhi... | |||||||||||||
Medical condition: Patients aged ≥ 18, of both gender, with advanced stage hepatocellular carcinoma, BCLC class B (intermediate stage, performance status-ECOG 0, multinodular HCC) or C (advanced stage, performance st... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001969-33 | Sponsor Protocol Number: TAK-242-2001 | Start Date*: 2020-05-28 | |||||||||||
Sponsor Name:Akaza Bioscience Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Proof-of-Concept, Phase 2a Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Intravenous TAK-242 in Subj... | |||||||||||||
Medical condition: Acute Alcoholic Hepatitis Causing Decompensation of Alcohol related Cirrhosis and Acute-on-Chronic Liver Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000974-22 | Sponsor Protocol Number: MRX-701 | Start Date*: 2021-01-29 | |||||||||||
Sponsor Name:Mirum Pharmaceuticals Inc. | |||||||||||||
Full Title: Randomized, Double-blind, Placebo-Controlled Phase 2 Study to Evaluate the Efficacy and Safety of Maralixibat in the Treatment of Subjects with Biliary Atresia after Hepatoportoenterostomy | |||||||||||||
Medical condition: Biliary atresia (BA) is a rare, inflammatory condition of the biliary tree that presents in the first weeks of life and leads to bile duct obstruction and consequent liver injury, fibrosis and cirr... | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) PL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002300-24 | Sponsor Protocol Number: 6.0 | Start Date*: 2015-03-20 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Albumin To prevenT Infection in chronic liveR failurE (ATTIRE) | |||||||||||||
Medical condition: Liver cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004619-36 | Sponsor Protocol Number: TS-102 | Start Date*: 2015-03-11 | ||||||||||||||||
Sponsor Name:Biocompatibles UK Ltd. | ||||||||||||||||||
Full Title: A Phase III Clinical Trial Evaluating TheraSphere® in Patients with Metastatic Colorectal Carcinoma of the Liver who have Failed First Line Chemotherapy | ||||||||||||||||||
Medical condition: Metastatic Colorectal Carcinoma of the Liver | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005376-34 | Sponsor Protocol Number: BEV-ONCO2012 | Start Date*: 2012-12-20 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Randomized Phase 2 study comparing pathological responses observed on colorectal cancer metastases resected after preoperative treatment combining bevacizumab with FOLFOX or FOLFIRI. | ||
Medical condition: Resecable Metastatic Cororectal Cancer. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017192-26 | Sponsor Protocol Number: BUILT_01 | Start Date*: 2012-06-21 | |||||||||||||||||||||
Sponsor Name:Free State of Bavaria represented by Regensburg University represented by Regensburg University Hospital represented by | |||||||||||||||||||||||
Full Title: A 3-Armed Prospective Randomized Controlled, Open-Labeled Phase III Trial to Evaluate Late Introduction of Cyclosporine or Everolimus versus a 5-day Delay of Cyclosporine in Combination with MMF in... | |||||||||||||||||||||||
Medical condition: Liver transplantation, renal function, high MELD scores, infections, "bottom-up" immunosuppression | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001536-36 | Sponsor Protocol Number: EARLY-HEP-C | Start Date*: 2016-08-03 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Efficacy of GZR/EBR in Early Chronic Hepatitis C in HIV/HCV co-infected patients | ||||||||||||||||||
Medical condition: Early Chronic Hepatitis C in HIV/HCV co-infected patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001402-18 | Sponsor Protocol Number: CIR-MSC-2014-01 | Start Date*: 2015-05-07 | |||||||||||
Sponsor Name:ALEJANDRA GARCIA BOTELLA | |||||||||||||
Full Title: CD133 + CELL INFUSION IN PATIENTS WITH COLORECTAL LIVER ORIGIN METASTASES GOING TO BE SUBMITTED TO A MAJOR LIVER RESECTION | |||||||||||||
Medical condition: patients with liver metastases from colorectal carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005136-16 | Sponsor Protocol Number: Cortisave-001 | Start Date*: 2017-06-02 |
Sponsor Name:CUB Erasme Hospital | ||
Full Title: Corticosteroids in patients with severe alcoholic hepatitis patients in early spontaneous improvement | ||
Medical condition: severe alcoholic hepatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000963-41 | Sponsor Protocol Number: 104-06-301 | Start Date*: 2008-12-03 | |||||||||||
Sponsor Name:CELSION CORPORATION | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blinded, Dummy-Controlled Study of the Efficacy and Safety of ThermoDox (Thermally Sensitive Liposomal Doxorubicin) in Combination with Radiofrequency Ablation (R... | |||||||||||||
Medical condition: patients with Non-Resectable Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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