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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT03285217 Completed - Sarcopenia Clinical Trials

HMB for Denutrition in Patients With Cirrhosis (HEPATIC)

HEPATIC
Start date: October 15, 2017
Phase: N/A
Study type: Interventional

Cirrhosis is a late stage of hepatic fibrosis caused by many forms of liver diseases and conditions, such as hepatitis and chronic alcoholism. The World Health Organization (WHO) has reported that this condition accounts for 1.8% of all deaths in Europe (170,000 deaths/year). Patients with cirrhosis are characterized by severe metabolic alterations, which converge in a malnutritional state. Malnutrition encompasses glucose intolerance, chronic inflammation, altered gut microbiota, reduced muscle mass (sarcopenia), as well as loss and dysregulation of adipose tissue (adipopenia). Malnutrition is the most frequent complication that adversely affects the outcomes of cirrhotic patients. Yet, despite its clinical repercussions and potential reversibility, there are no effective therapies because our limited understanding of the mechanisms underlying this altered metabolism. β-hydroxy β-methylbutyrate (HMB) is a naturally produced substance regarded as safe and effective in preventing muscle loss during chronic diseases. Previous studies have indicated some beneficial effects of HMB itself or its parent metabolite, leucine, on adipose tissue, glucose intolerance, inflammation, and gut microbiota. This study aims to translate those beneficial effects to cirrhotic patients. The investigators hypothesize that HMB can improve cirrhosis-related metabolic abnormalities through its pleiotropic effects. The goals of this study are: i) to perform a randomized clinical trial to evaluate the efficacy of HMB, administered as nutritional supplementation, on clinical symptoms of cirrhosis. ii) to uncover the precise metabolic pathways that underlie HMB action, with a special focus on muscle, adipose tissue, and gut microbiota.

NCT ID: NCT03278925 Active, not recruiting - Cirrhosis Clinical Trials

Defined Green Tea Catechin Extract in Preventing Liver Cancer in Participants With Cirrhosis

Start date: August 9, 2018
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of defined green tea catechin extract and to see how well it works in preventing liver cancer in participants with cirrhosis. Higher levels of the molecule gamma-OHPdG may be found in participants with cirrhosis, which may mean a higher risk of the development of liver cancer. Defined green tea catechin extract may work better to lower levels of gamma-OHPdG and prevent the development of liver cancer.

NCT ID: NCT03277651 Recruiting - Cirrhosis Clinical Trials

Noninvasive Diagnostic Platform for Liver Fibrosis and Portal Hypertension

Start date: October 9, 2017
Phase: N/A
Study type: Observational

This study is to establish a noninvasive diagnostic platform based on hemodynamic information for the assessment of liver fibrosis, liver cirrhosis and portal hypertension.

NCT ID: NCT03246048 Completed - Cirrhosis Clinical Trials

Long Term Follow-up of Hepatitis C Cured Patients

Start date: January 2016
Phase:
Study type: Observational

Objectives: The general objective of the present project is to gain a better understanding of disease outcome in cACLD patients treated with the new oral DAA. In particular, the project will focus on: - To evaluate the long term prognosis of patients with compensated advanced chronic liver disease (cACLD) who achieve sustained virological response (SVR) after the new oral direct-acting antiviral agents (DAA), and determine clinical and elastographic basal and follow-up parameters to identify low and high risk groups of developing liver-related decompensation. Methods: Prospective cohort study in patients with cACLD in whom basal and annual clinical features and liver stiffness measurements (LSM) will be performed, and survival free of liver-related events will be analyzed.

NCT ID: NCT03242798 Completed - Malnutrition Clinical Trials

Assessment of Nutritional Status of Patients With Liver Cirrhosis

Start date: March 3, 2016
Phase:
Study type: Observational

Cirrhosis is the twelfth leading cause of death worldwide. Malnutrition is prevalent among cirrhotic patients and is an important prognostic factor. Nutritional assessment is therefore crucial for identifying patients at risk or with already established malnutrition and refer them for nutritional intervention and support. In the current literature, nutritional assessment of cirrhotic patients is performed using several tools and methods. However their accuracy is widely affected by the underline disease and its complications. In addition, for the majority of the parameters under study, no gold standard tools and methods have been established so far. Studies on nutritional assessment in cirrhosis usually focus on one or few aspects of nutritional status and not on a full nutritional assessment combining information from medical, biochemical, nutritional, and body composition variables. Hence, the present study aims at a thorough assessment of the nutritional status of 170 cirrhotic patients using multiple widely available tools and methods, in order to assess their accuracy and estimate the prevalence of multiple malnutrition phenotypes such as undernutrition, sarcopenia, sarcopenic obesity and cachexia.

NCT ID: NCT03225677 Recruiting - Cirrhosis Clinical Trials

Novel Tracer Methods to Evaluate Muscle Protein Metabolism in Cirrhosis

Start date: July 3, 2017
Phase:
Study type: Observational

To determine the rate and mechanisms of skeletal muscle protein synthesis and breakdown in cirrhotic patients by using multiple tracers and single muscle biopsies.

NCT ID: NCT03195634 Not yet recruiting - Cirrhosis Clinical Trials

WFA+M2BP in Evaluation of Portal Hypertension and Clinical Outcome in Patients With Liver Cirrhosis

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

Portal hypertension is a common complication of chronic liver diseases and is responsible for most clinical consequences of cirrhosis. measurement of the hepatic venous pressure gradient(HVPG) is the gold standard for evaluating the presence and severity of portal hypertension, this technique is considered invasive and is not routinely performed in all centers. Wisteria floribunda agglutinin-positive human Mac-2 binding protein (WFA+-M2BP) is a secreted N-glycoprotein, which has been reported as a novel marker in assessing liver fibrosis.However, the correlation of WFA+-M2BP with HVPG is unclear.The aim of this study was to explore the relationship between WFA+-M2BP and HVPG.

NCT ID: NCT03176966 Completed - Cirrhosis Clinical Trials

Ropinirole for the Treatment of Muscle Cramps in Patients With Cirrhosis

Start date: September 2, 2016
Phase: Phase 4
Study type: Interventional

The investigator's aim is to compare the efficacy of Ropinirole (Requip) to vitamin E in the treatment of muscle cramps in cirrhotic patients.

NCT ID: NCT03176797 Enrolling by invitation - Cirrhosis Clinical Trials

Quantitative Diagnosis of Liver Fibrosis on Multiparametric MRI

Start date: May 3, 2017
Phase: N/A
Study type: Interventional

Early diagnosis and treatment of liver fibrosis can repress or delay the development of cirrhosis and hepatocellular carcinoma. The purpose of this pilot study is to evaluate non-invasive multiparametric magnetic resonance imaging (MRI) techniques in the detection and grading of liver fibrosis, so that patients can be treated in time. These techniques combined could reach high diagnostic performance for detection of liver fibrosis, and could decrease the number of liver biopsies.

NCT ID: NCT03154476 Completed - Cirrhosis Clinical Trials

Role of Sildenafil for Fontan Associated Liver Disease (SiFALD) Study

SiFALD
Start date: July 5, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the medication, sildenafil (also known as Revatio), can slow or stop the progression of liver disease in patients who previously had a Fontan operation.