Clinical Trials Logo

Liver Failure clinical trials

View clinical trials related to Liver Failure.

Filter by:

NCT ID: NCT04186572 Not yet recruiting - Clinical trials for Acute-On-Chronic Liver Failure

Usefulness of the Variation of the CLIF-C ACLF Score in Patients With Acute on Chronic Liver Failure

ARIHAC
Start date: December 2019
Phase:
Study type: Observational [Patient Registry]

Patients with Acute on Chronic Liver Failure (ACLF) have high short-term mortality. The use of a severity score could define the patient's prognosis and would help determine in whom the treatment is effective or futile.

NCT ID: NCT04051437 Not yet recruiting - Cirrhosis, Liver Clinical Trials

Plasma Exchange in Acute on Chronic Liver Failure

PLEXAR
Start date: August 15, 2019
Phase: Phase 3
Study type: Interventional

Acute on chronic liver failure (ACLF) is a distinct syndrome in patients with chronic liver disease with rapid clinical deterioration and has high short term mortality within one month.Despite aggressive clinical care, only half of the patients could survive an episode of ACLF. The investigators hypothesized that the early treatment with therapeutic plasma exchange with plasma and albumin in ACLF patients might improve overall survival in carefully selected patients by removing cytokines, chemokines and toxic substances.

NCT ID: NCT03944330 Not yet recruiting - Nutrition Clinical Trials

A Study on Nutrition Support Therapy of Patients With Liver Failure

Start date: May 10, 2019
Phase: N/A
Study type: Interventional

This study is a Clinical trial to assess the efficacy of nutrition support therapy of patients with liver failure. Patients were randomized to one of 2 groups to receive different nutrition and energy support treatment.

NCT ID: NCT03863002 Not yet recruiting - Clinical trials for Liver Failure, Acute on Chronic

Safety and Efficacy of Mesenchymal Stem Cell Transplantation for Acute-on-Chronic Liver Failure

Start date: October 1, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Safety and Efficacy of Mesenchymal Stem Cell Transplantation for Acute-on-Chronic Liver Failure

NCT ID: NCT03761238 Not yet recruiting - Clinical trials for Liver Failure as A Complication of Care

Early Liver Support With MARS in Post-hepatectomy Liver Failure

ELISH
Start date: March 15, 2019
Phase: N/A
Study type: Interventional

This is a prospective, randomized, open-label, multicentre study involving European centers with experience in the management of PHLF to assess the impact of early liver support with MARS on survival in patients with post-hepatectomy liver failure (PHLF).

NCT ID: NCT03560414 Not yet recruiting - Hepatic Failure Clinical Trials

The Plasma Diafiltration Therapy of Hepatic Failure

Start date: June 2018
Phase: N/A
Study type: Interventional

At present, there is no comparative study between the simple plasma exchange and plasma diafiltration (PDF), and no further exploration of optimal plasma dose in PDF treatment. Therefore, this prospective randomized cohort study aims to compare the safety and effectiveness of the tree groups(simple plasma exchange group, conventional PDF treatment group, less plasma PDF treatment group)by collecting SOFA score, 3-month survival rate, MELD score, and the times of artificial liver treatment , blood cell variables, cytokines(e.g. TNFα ), pre- and post-treatment plasma ammonia levels. Thus, it is to provide a safer and more effective artificial liver treatment with less plasma dose.

NCT ID: NCT03285867 Not yet recruiting - Clinical trials for Hepatocellular Carcinoma

Liver Stiffness Measurement (LSM) in Predicting Progress of Liver Fibrosis After TACE for Hepatocellular Carcinoma

Start date: June 25, 2018
Phase:
Study type: Observational

Objective: To evaluate the efficacy of preoperative liver stiffness measurement(LSM) by FibroScan in predicting the progress of liver fibrosis and prognosis after transcatheter arterial chemoembolization (TACE) in hepatocellular carcinoma (HCC). Background: Progress of liver fibrosis and liver failure and related poor prognosis after TACE which are not completely predictable by current method including Child-Pugh Classification. LSM is used to calculate the degree of liver fibrosis and is affected by several liver injury, e.g. elevated Alanine aminotransferase(ALT), Aspartate transaminase(AST) and Bilirubin et al. The investigators assume that LSM could be use to predict progress of liver fibrosis and adverse effects after TACE in HCC. Methods: At least 200 patients will be recruited in this prospective observational study with preoperative LSM, demographic, laboratory, radiological and other treatment-related factors. Participants will be followed up till death or to the end of study no matter the liver failure occurs or not. Data will be analyzed to build a mathematical predicting model. Research hypothesis:TACE is related to progress of liver fibrosis and a mathematical model with LSM is able to predict the risk of liver failure and prognosis in HCC.

NCT ID: NCT03084198 Not yet recruiting - Clinical trials for Liver Failure, Acute

Safety and Efficacy of hiHep Bioartificial Liver Support System to Treat Acute Liver Failure

Start date: June 2017
Phase: N/A
Study type: Interventional

This study tend to evaluate safety and efficacy of hiHep bioartificial liver support system in treating acute liver failure.

NCT ID: NCT02812121 Not yet recruiting - Liver Failure Clinical Trials

UC-MSC Infusion for HBV-Related Acute-on-Chronic Liver Failure

Start date: June 2016
Phase: Phase 2
Study type: Interventional

Hepatitis B virus (HBV)-related acute-on-chronic liver failure (ACLF) is a severe disease with high mortality. Our previous study have demonstrated that peripheral infusion of bone marrow-derived mesenchymal stromal cells (MSCs) weekly for 4 times is safe and improves 24 weeks survival rate of ACLF patients. In this study, we intend to assess the safety and efficacy of umbilical cord blood derived MSCs for HBV-related ACLF patients.

NCT ID: NCT01961440 Not yet recruiting - Liver Failure Clinical Trials

Prognosis Scoring System for Acute-on-Chronic Liver Failure

Start date: October 2013
Phase: N/A
Study type: Observational

This research is to establish a simple and practical system to predict the prognosis of sever hepatitis B.Seven factors (level of serum total bilirubin, prothrombin time, severity of hepatic encephalopathy, hepatorenal syndrome,ascites ,infection and size of liver) which were easier to evaluate and more influential, were included to establish a prognosis scoring system.The scorings of a new score system and MELD were graded at the same time in the patients with sever hepatitis B. And then the distribution figures of survival rates and mortality rates were done according to the scores from low to high. The features of distribution figures of two score system in survival rates and mortality rates and significances of clinical application in certain score were interpreted.