- Trials with a EudraCT protocol (536)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
536 result(s) found for: Liver Cirrhosis.
Displaying page 2 of 27.
EudraCT Number: 2012-002890-71 | Sponsor Protocol Number: RifaxNK150612 | Start Date*: 2012-08-16 | |||||||||||
Sponsor Name:Flemming Bendtsen | |||||||||||||
Full Title: Intestinal decontamination with rifaximin. Effects on the inflammatory and circulatory state in patients with cirrhosis and ascites - A randomised controlled clinical study | |||||||||||||
Medical condition: Liver cirrhosis of any etilogy, complicated by decompensation and classified as Child-Pugh B or C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006393-14 | Sponsor Protocol Number: UDT-1/PHT | Start Date*: 2007-10-23 | ||||||||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | ||||||||||||||||||
Full Title: Double-Blind, Randomised, Parallel-Group, Placebo-Controlled, Multi-Centre Phase II Clinical Study on the Efficacy and Safety of Different Doses of Udenafil in Cirrhotic Patients with Portal Hypert... | ||||||||||||||||||
Medical condition: Portal hypertension, liver cirrhosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) LT (Completed) CZ (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000488-34 | Sponsor Protocol Number: PVTRIFA2017 | Start Date*: 2017-06-14 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: RIFAXIMIN BLUNTED HIGHER LEVELS OF ENDOTOXIN IN CIRRHOSIS PATIENTS: A RANDOMIZED, DOUBLE BLIND, SHORT TERM INTERVENTIONAL TRIAL. | |||||||||||||
Medical condition: PATIENTS WITH CIRRHOSIS CHILD PUGH B or C Classes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005679-33 | Sponsor Protocol Number: KKSH-042 | Start Date*: 2011-01-20 | ||||||||||||||||
Sponsor Name:Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg | ||||||||||||||||||
Full Title: Influence of the selective endothelin receptor-blocker Ambrisetan on the portal pressure in patients with cirrhosis | ||||||||||||||||||
Medical condition: Portal hypertension and hepatic cirrhosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002940-86 | Sponsor Protocol Number: SELLIFA-02 | Start Date*: 2007-08-24 | |||||||||||
Sponsor Name:Cliniques Universitaires Saint-Luc – Université catholique de Louvain | |||||||||||||
Full Title: Sepsis, Endothelial function, and Lipids in critically ill patients with Liver Failure (SELLIFA). Nutritional sub-study : Randomized controlled trial comparing the tolerance on lipid metabolism and... | |||||||||||||
Medical condition: Liver failure, Liver cirrhosis, critical illness, total nutritional support | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004809-33 | Sponsor Protocol Number: BETA | Start Date*: 2015-03-09 | ||||||||||||||||
Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | ||||||||||||||||||
Full Title: Albumin infusion effects in patients with cirrhosis hepatic encephalopathy | ||||||||||||||||||
Medical condition: hepatic encephalopathty | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024651-86 | Sponsor Protocol Number: TEHYLIC | Start Date*: 2011-05-30 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Randomized Trial, Masked, and Placebo Controlled to Assess the Effects of Sapropterin on Hepatic and Systemic Hemodynamics in Patients With Liver Cirrhosis and Portal Hypertension | ||||||||||||||||||
Medical condition: Cirrosis hepática, Hipertensión portal | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003547-36 | Sponsor Protocol Number: NRL972-09/2008- (CHBC) | Start Date*: 2009-02-12 | |||||||||||
Sponsor Name:Norgine Ltd | |||||||||||||
Full Title: An open study to investigate the effects of chronic hepatitis B or C on the pharmacokinetics of cholyl-lysyl-fluorescein (NRL972) before, during and after standard treatment | |||||||||||||
Medical condition: In-vivo diagnostic marker for liver dysfunction. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002778-35 | Sponsor Protocol Number: 87RI18_0008 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:CHU de Limoges | |||||||||||||
Full Title: Description of the evolution of plasma and urinary concentrations of iohexol in a cirrhotic patient population. "Pilot study on 9 patients" | |||||||||||||
Medical condition: Patients with advanced liver disease, with potential indication for liver transplantation, with or without ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002409-75 | Sponsor Protocol Number: Dota-PrimoLIV | Start Date*: 2014-01-06 | ||||||||||||||||
Sponsor Name:Charite | ||||||||||||||||||
Full Title: Intra-individual, comparison of the MRI contrast agents gadoxetic acid (Primovist®) versus gadoterate meglumine (Dotarem®) in liver MRI of patients with HCC and underlying cirrhosis | ||||||||||||||||||
Medical condition: Patients with liver cirrhosis and diagnosis of hepatocellular carcinoma based on noninvasive HCC diagnostic (EASL) criteria | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017819-16 | Sponsor Protocol Number: OP-GIB | Start Date*: 2011-08-22 | ||||||||||||||||
Sponsor Name:Juan Cordoba | ||||||||||||||||||
Full Title: Efectos de la administración de ornitina-fenilacetato (OCR-002) en pacientes con cirrosis y hemorragia digestiva alta. Effects of the administration of ornithine phenylacetate (OP, OCR-002) in pati... | ||||||||||||||||||
Medical condition: Hemorragia digestiva en pacientes con cirrosis hepática | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002166-20 | Sponsor Protocol Number: AMELIORATE | Start Date*: 2012-02-08 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Treatment of hepatorenal syndrome with terlipressin infusion adjusted to hemodynamic response | ||||||||||||||||||
Medical condition: Hepatorenal syndrome (HRS) type 1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005723-14 | Sponsor Protocol Number: MACHT | Start Date*: 2008-04-21 | |||||||||||
Sponsor Name:Fundació Clinic per a la recerca biomèdica | |||||||||||||
Full Title: EFECTO DE LA ADMINISTRACIÓN PROLONGADA DE ALBÚMINA Y MIDODRINA EN LA PREVENCIÓN DE COMPLICACIONES EN PACIENTES EN LISTA DE ESPERA DE TRASPLANTE HEPÁTICO Midodrine and Albumin for CirrHotic patients... | |||||||||||||
Medical condition: Pacientes afectos de cirrósis hepática en lista de espera para trasplante Hepático | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006577-30 | Sponsor Protocol Number: D4326C00003 | Start Date*: 2022-09-21 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Two Part Phase IIa/b Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Dose-ranging Study to Assess Efficacy, Safety, and Tolerability of the Combination of Zibotentan and... | |||||||||||||
Medical condition: Liver cirrhosis with features of portal hypertension. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) AT (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) DE (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: 2009-010396-25 | Sponsor Protocol Number: PREDESCI | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:Càndid Villanueva | |||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, doble-ciego, controlado con placebo, sobre la eficacia del tratamiento con beta-bloqueantes pra aprevenir la descompenzación de la cirrosis con hipertensión po... | |||||||||||||
Medical condition: Cirrosis hepática con hipertensión portal clínicamente significativa (mayor o igual a 10 mm Hg) sin descompensaciones como varíces esofágicas, ascitis, o encefalopatía hepática. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012592-10 | Sponsor Protocol Number: 09-057 | Start Date*: 2009-07-23 | |||||||||||
Sponsor Name:CHU Caen | |||||||||||||
Full Title: Méthode d’évaluation de l’aptitude à la conduite chez des patients souffrant de pathologies de l’éveil: cirrhose avec ou sans encéphalopathie (AutoSoP "foie"). | |||||||||||||
Medical condition: cirrhose | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012919-17 | Sponsor Protocol Number: P071220 | Start Date*: 2009-11-12 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude multicentrique randomisée en double insu des effets de l'administration de norfloxacine ou d'un placebo sur la survie des malades atteints de cirrhose avec une insuffisance hépatocellulaire | |||||||||||||
Medical condition: Malades atteints de cirrhose avec une insuffisance hépatocellulaire de grade C de Child-Pugh | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
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: 2019-005008-16 | Sponsor Protocol Number: STOPPIT-01 | Start Date*: 2021-03-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Stop of proton-pump inhibitor treatment in patients with liver cirrhosis – a double-blind, placebo-controlled trial | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Liver cirrhosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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