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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT02964195 Recruiting - Cirrhosis Clinical Trials

Efficacy of Rifaximin in Treatment of Cirrhotic Gastroesophageal Variceal Bleeding

EoR-GEVB
Start date: November 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the efficacy of Rifaximin in the treatment of cirrhotic gastroesophageal variceal bleeding.

NCT ID: NCT02931812 Recruiting - Cirrhosis Clinical Trials

Feeding Behavior and Taste Sensitivity Before and After Liver or Renal Transplantation

GREFFE
Start date: May 2014
Phase:
Study type: Observational

This study evaluates the influence of the taste sensitivity, of food preferences and of the reward system on the energetic balance before and after liver transplantation in cirrhotic patients and after kidney transplantation in renal failure patients

NCT ID: NCT02757170 Recruiting - Cirrhosis Clinical Trials

Assessment of Coagulation Abnormalities in Acute on Chronic Liver Failure Patients Using Thromboelastography

Start date: July 2015
Phase: Phase 4
Study type: Interventional

Patients of acute & chronic liver failure have long been assumed to have coagulopathy & are given blood products prophylactically as well as during various interventions. But these patients rarely have spontaneous bleed except variceal bleed. Conventional coagulation parameters are insufficient to assess coagulation status of these patients because they reflect only a certain element of coagulation cascade while thromboelastography (TEG) gives a comprehensive report of hemostatic profile including platelet function. Studies using TEG have suggested that defects in prohemostatic drivers are counterbalanced by changes in antihemostatic drivers creating a rebalance in these patients. Acute on chronic failure is a entity with acute decompensation on underlying chronic liver failure. Since there is paucity of data regarding coagulation abnormalities in these patient, study is needed to assess predictability power of TEG in these patients with respect to coagulation abnormalities in patient with ALF and CLD ( cirrhosis) and healthy controls.

NCT ID: NCT02755701 Recruiting - Cirrhosis Clinical Trials

The Effect of Branched-chain Amino Acid on the Improvement of Serum Albumin Level in Cirrhotic Patients With Ascites

Start date: July 2016
Phase: Phase 4
Study type: Interventional

To compare the efficacy of branched-chain amino acid in serum albumin level in cirrhotic patients with ascites.

NCT ID: NCT02693951 Recruiting - Cirrhosis Clinical Trials

Efficiency and Safety of Prophylactic Use of Antibiotics in Endoscopic Injection of Tissue Adhesive in Gastric Varices

Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the efficiency and safety of prophylactic use of antibiotics in endoscopic injection of tissue adhesive in gastric varices.

NCT ID: NCT02643212 Recruiting - Cirrhosis Clinical Trials

Multicenter Prospective Randomized Trial of the Effect of Rivaroxaban on Survival and Development of Complications of Portal Hypertension in Patients With Cirrhosis

CIRROXABAN
Start date: May 2016
Phase: Phase 3
Study type: Interventional

The main objective of the study will determine if patients with liver cirrhosis, anticoagulation free survival improves hypertension decompensation portal and / or transplantation without serious side effects. For it is conduct a double-blind multicenter clinical trial in which patients will be randomized to receive Rivaroxaban or placebo. It included 160 patients with liver cirrhosis and insufficiency mild to moderate hepatic. It will also analyze and develop secondary endpoint portal vein thrombosis. The confirmation of our hypothesis would lead to a radical change in treatment of patients with cirrhosis include treatment with Rivaroxaban in its drove.

NCT ID: NCT02638415 Recruiting - Cirrhosis Clinical Trials

The Effect of Hepatic Vein Pressure Gradient(HVPG)-Guided Therapy in Cirrhotic Patients With Esophagogastric Varices

Start date: December 2015
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare the effect of HVPG-guided individualized therapy and non-HVPG guided traditional therapy in cirrhotic patients for secondary prophylaxis.

NCT ID: NCT02476695 Recruiting - Cirrhosis Clinical Trials

FibroTouch Non-invasive Evaluation of Liver Fibrosis and Cirrhosis

Start date: May 2014
Phase: N/A
Study type: Observational

This prospective and multicenter study is to determine the diagnostic performance (accuracy, specificity and sensitivity) of transient elastography (FibroTouch) for liver fibrosis assessment in chronic hepatitis B (CHB) patients using ROC analysis, and liver biopsy as the reference. Approximately 600 patients will be enrolled to guarantee 500 final statistical cases; and ≥100 cases are required for fibrosis stage S0/1, S2, S3 and S4 (compensatory stage of cirrhosis), respectively. For each stage, the case is assigned as equally as possible.

NCT ID: NCT02427906 Recruiting - Cirrhosis Clinical Trials

Effect of Transjugular Intrahepatic Portosystemic Shunt on Gut Microbiota in Cirrhotic Patients

Start date: August 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine the effect of transjugular intrahepatic portosystemic shunt on gut microbiota and associated inflammatory factors in cirrhotic patients.

NCT ID: NCT02401490 Recruiting - Cirrhosis Clinical Trials

Albumin Infusion Effects in Mortality in Patients With Cirrhosis and Hepatic Encephalopathy

BETA
Start date: April 2015
Phase: Phase 4
Study type: Interventional

To assess whether albumin administration after an episode of hepatic encephalopathy (≥ grade II) improves survival at 90 days (mortality endpoint treated as a composite endpoint death and/ or liver transplantation).