- Trials with a EudraCT protocol (1,286)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,286 result(s) found for: Liver failure.
Displaying page 1 of 65.
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001705-21 | Sponsor Protocol Number: 030705 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: Phase II study to evaluate hepatic function and clinical aspects in patients with severe hepatic cirrhosis treated with multiple cycle of stem cells mobilisation by G-CSF administration. | |||||||||||||
Medical condition: Hepatic cirrhosis with severe liver dysfunction | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005108-33 | Sponsor Protocol Number: Short2-INF-RIBA | Start Date*: 2005-02-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: RANDOMISED CONTROLLED STUDY ON EARLY RENSPONSE TO COMBINED ANTIVIRAL THERAPY IN CHRONIC H EPATITIS C PATIENTS GENOTIPE 2 AND 3 WITH HCV-RNA NEGATIVE WEEK 4 | |||||||||||||
Medical condition: SOSTAINED BIOCHEMICAL AND VIROLOGICAL RESPONSE TO COMBINADET THERAPY PEGILATED RIBAVIRIN IN CHRONIC HEPATITIES PATIENTS G 2 AND 3 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005112-83 | Sponsor Protocol Number: Short1/4-INF-RIBA | Start Date*: 2005-02-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: RANDOMISED CONTROLLED STUDY ON EARLY RESPONSE TO COMBINED ANTIVIRAL THERAPY IN CHRONIC EPATITES C PATIENT GENOTIPE 1 AND 4 WITH HCV RNA NEGATIVE WEEK 6 | |||||||||||||
Medical condition: SOSTAINED BIOCHEMICAL AND VIROLOGICAL RESPONSE TO COMBINATED THERAPY PEGILATED RIBAVIRIN IN CHRONIC EPATITIES PATIENTS G 1 AND 4 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020657-14 | Sponsor Protocol Number: ALF-5755_P2_ALF | Start Date*: 2011-07-04 | |||||||||||
Sponsor Name:Alfact Innovation | |||||||||||||
Full Title: A multicentre, double-blind, randomized, placebo-controlled study to evaluate the efficacy and the safety of ALF-5755 in patients with nonacetaminophen severe acute hepatitis and early stage acute ... | |||||||||||||
Medical condition: Acute liver failure | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002079-16 | Sponsor Protocol Number: E2013_PK_CASPO70_LIVERFAILURE | Start Date*: 2013-09-05 | |||||||||||
Sponsor Name:Hospital Erasme | |||||||||||||
Full Title: Pharmacokinetics of Caspofungin after one dose in patients with liver failure. | |||||||||||||
Medical condition: The pharmacokinetics parameters of caspofungin will be studied for the patient admitted for alcoholic hepatitis or decompensated cirrhosis (Child-Pugh score 7-15). | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004031-23 | Sponsor Protocol Number: E2012AILIVER | Start Date*: 2014-08-26 | |||||||||||
Sponsor Name:Hopital Erasme | |||||||||||||
Full Title: Serum pharmacokinetics of Caspofungin in patients with liver failure. | |||||||||||||
Medical condition: The patient admitted for alcoholic hepatitis or decompensated cirrhosis (Child-Pugh score of 10-15) presenting with invasive aspergillosis (proven or probable) and treated by caspofungin. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003023-20 | Sponsor Protocol Number: UCL-PLTP-002 | Start Date*: 2008-09-11 | |||||||||||
Sponsor Name:Cliniques universitaires Saint-Luc | |||||||||||||
Full Title: TACROLIMUS – DACLIZUMAB - MYCOPHENOLATE MOFETIL IMMUNE PROPHYLAXIS IN PEDIATRIC LIVER TRANSPLANTATION. An open, pilot, investigator-driven study in 20 recipients | |||||||||||||
Medical condition: Liver transplantation | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008754-23 | Sponsor Protocol Number: CILT08 | Start Date*: 2009-12-16 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Göttingen | ||||||||||||||||||||||||||||
Full Title: A Therapeutic Exploratory Study to Determine the Efficacy and Safety of Calcineurin-Inhibitor-Free de-novo Immunosuppression after Liver Transplantation. | ||||||||||||||||||||||||||||
Medical condition: Patients with renal dysfunction undergoing liver transplantation | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000316-29 | Sponsor Protocol Number: 3571 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: Hepatocytes co-encapsulated with mesenchymal stromal cells in alginate microbeads for the treatment of acute liver failure in paediatric patients: HELP study | |||||||||||||
Medical condition: Acute liver failure in paediatric patients | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000837-39 | Sponsor Protocol Number: CCD01 | Start Date*: 2007-08-15 | |||||||||||
Sponsor Name:Cytonet GmbH & Co. KG | |||||||||||||
Full Title: Open, randomized, prospective, controlled, multicentre study to evaluate the efficacy and safety of multiple intraportal applications of liver cell suspension in patients with acute liver failure n... | |||||||||||||
Medical condition: Acute Liver Failure Subgroups of patients with indications falling under ICD classification codes:K70.4, K71, K72, K75, K76, K77 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016176-78 | Sponsor Protocol Number: 2009-016176-78 | Start Date*: 2010-02-08 | |||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||||||||||||
Full Title: Terapy with everolimus in liver transplant. | |||||||||||||||||||||||
Medical condition: liver transplant | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020212-11 | Sponsor Protocol Number: 2010-338 | Start Date*: 2010-09-09 | |||||||||||
Sponsor Name:Overlæge dr.med. Frederik Grønhøj | |||||||||||||
Full Title: Enkelt dosis (single dosis) farmakokinetik af 9-cis-retinoic acid (Alitretinoin, Toctino®) hos patienter med moderat til svær lever insufficiens. | |||||||||||||
Medical condition: At undersøge enkeltdosis-farmakokinetikken af 9-cis-RA (Alitretinoin, Toctino®) og dets metaboliter hos patienter med moderat til svær leverinsufficiens og frivillige raske forsøgspersoner. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002226-36 | Sponsor Protocol Number: N-003-CRD002 | Start Date*: 2016-11-04 | ||||||||||||||||
Sponsor Name:Noorik Biopharmaceuticals AG | ||||||||||||||||||
Full Title: A double-blind, placebo-controlled, escalating-dose study of the effect of N-003 on renal function, pharmacodynamics, pharmacokinetics, safety and tolerability in patients with advanced liver disease. | ||||||||||||||||||
Medical condition: Decompensated cirrhosis of the liver | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001177-32 | Sponsor Protocol Number: HEP101 | Start Date*: 2016-08-09 | ||||||||||||||||
Sponsor Name:Promethera Biosciences | ||||||||||||||||||
Full Title: Multicenter Phase II Safety and Preliminary Efficacy Study of 2 dose regimens of HepaStem in Patients with Acute on Chronic Liver Failure | ||||||||||||||||||
Medical condition: The study will recruit cirrhotic patients who are hospitalized for Acute-on-chronic liver failure (ACLF) or Acute Decompensation at risk of developing ACLF. ACLF combines an acute deterioration of... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012763-34 | Sponsor Protocol Number: V.1 | Start Date*: 2009-12-28 |
Sponsor Name:Medizinische Universität Wien, Univ. Klinik für Anästhesie, Allg. Intensivmedizin u Schmerztherapie | ||
Full Title: Reversal of neuromuscular blockage in Patients with End Stage Hepatic Failure (listed for Liver Transplantation) | ||
Medical condition: Patients with liver-failure undergoing surgery and receiving Rocuronium. Sugammadex is approved for recovery of Rocuronium. There are to date no clinical data to Sugammadex in patients with liver ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-002567-42 | Sponsor Protocol Number: 5A | Start Date*: 2015-07-15 |
Sponsor Name:Stockholm County Council, Karolinska University Hospital Huddinge, Dept of Anesthesiology and Intensive Care | ||
Full Title: Predictors of albumin synthesis rate in severe liver failure. An open exploratory study in patients with chronic liver failure assessed for liver transplantation | ||
Medical condition: Severe chronic liver failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
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 | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (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... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003051-11 | Sponsor Protocol Number: HEP102-DHELIVER | Start Date*: 2019-12-04 | |||||||||||
Sponsor Name:Promethera Therapeutics | |||||||||||||
Full Title: Randomized, placebo-controlled, double blind, multi-centre Phase IIb study to evaluate the efficacy and safety of HepaStem in patients with Acute on Chronic Liver Failure (ACLF) - DHELIVER | |||||||||||||
Medical condition: Cirrhotic patients who are hospitalized for Acute on chronic liver failure (ACLF), ACLF combines an acute deterioration of liver function in an individual with pre-existing chronic liver disease a... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) LV (Trial now transitioned) LT (Trial now transitioned) SK (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) PL (Trial now transitioned) PT (Completed) EE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) SI (Completed) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
