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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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NCT ID: NCT05199259 Recruiting - Clinical trials for Hepatocellular Carcinoma

Multi-analyte Blood Test Clinical Trial

LIVER-1
Start date: March 1, 2022
Phase:
Study type: Observational

The objective of this study is the acquisition of whole blood samples and serum samples from participants with untreated Hepatocellular Carcinoma (HCC) and subjects undergoing Hepatocellular Carcinoma (HCC) surveillance. These samples will be used for research purposes to develop and validate the Helio multi-analyte blood test.

NCT ID: NCT05196867 Recruiting - Liver Diseases Clinical Trials

Liver Cancer Prevention Randomized Control Trial

Start date: February 11, 2022
Phase: N/A
Study type: Interventional

To determine the effectiveness of a behaviorally-based tailored disease management intervention in patients with fibrosis or steatosis and risk factors for cirrhosis.

NCT ID: NCT05187715 Recruiting - Liver Cirrhosis Clinical Trials

To Study the Safety and Efficacy of Simvastatin in Patients With Hepatopulmonary Syndrome in Cirrhosis.

Start date: February 26, 2022
Phase: N/A
Study type: Interventional

Hepatopulmonary syndrome (HPS) is a frequent pulmonary complication of end-stage liver disease that is characterized by decreased arterial oxygenation caused by intrapulmonary vascular dilatation. Due to the different diagnostic criteria used in different studies, its prevalence ranges from 4% to 47% in patients with cirrhosis. Main underlaying pathogensis for HPS being activation of macrophages which are responsible for iNOS, PDGF and VEGF release contributing to development of intrapulmonary vascular dilatation(IPVD) , and neoangiogenesis leading to anatomical shunt resulting decreased oxygenation. Sphingosine 1 phosphate (S1P) is an essential compound produced and secreted by endothelial cells, platelets and RBC's. S1P prevents adhesion, transmigration and release of inflammatory mediators from macrophages. S1P levels are decreased in cirrhotics. Simvastatin, a HMG CoA inhibitor has many pleotropic effects, Of which one is by agonizing the S1P response and improving oxygenation in HPS patients. Simvastatin at a optimal dose of 40mg/day for 6months. Pre and post simvastatin treatment related oxygenation changes and concurrently its effect on liver fibrosis will be evaluated.

NCT ID: NCT05185154 Recruiting - Liver Cirrhosis Clinical Trials

Natural Course and Prognosis of Hospitalized Patients With Cirrhosis

Start date: November 1, 2021
Phase:
Study type: Observational [Patient Registry]

The aim of this prospective study is to evaluate the natural course and prognosis of hospitalized patients with liver cirrhosis.

NCT ID: NCT05184283 Terminated - Clinical trials for Hepatocellular Carcinoma

Utilization of MAsS in Patients Undergoing LT for HCC

Start date: June 16, 2022
Phase:
Study type: Observational

The aim of this study is to determine the effects of liver transplantation and standard immunosuppression on body composition in patients with compensated cirrhosis and hepatocellular carcinoma.

NCT ID: NCT05181826 Recruiting - Cancer Clinical Trials

Collection of Blood From Healthy Patients, Patients With Benign Disease and Patients With Cancer

ELITE
Start date: May 21, 2019
Phase:
Study type: Observational

To acquire blood samples from subjects for various purposes, including: i) determining the sensitivity and specificity of select DNA methylation markers for the detection of various types of cancer, ii) identifying benign conditions that may induce false positive or false negative results, and iii) defining the effects of potential interfering substances, such as chemotherapy drugs.

NCT ID: NCT05181332 Recruiting - Cirrhosis Clinical Trials

Predictive Models of Hepatic Decompensation and Survival Outcomes in Pediatric Patients With Cirrhosis

Start date: January 1, 2021
Phase:
Study type: Observational

The aim of this study was to developed and validated models to predict hepatic decompensation and survivals in pediatric patients with cirrhosis and compared these models with currently available models.

NCT ID: NCT05180162 Recruiting - Pulmonary Fibrosis Clinical Trials

Imaging of Pathologic Fibrosis Using 68Ga-FAP-2286

Start date: December 9, 2021
Phase: Phase 1
Study type: Interventional

This is a single arm prospective pilot trial that evaluates the ability of a novel imaging agent (68Ga-FAP-2286) to identify pathologic fibrosis in the setting of hepatic, cardiac and pulmonary fibrosis. FAP-2286 is a peptide that potently and selectively binds to Fibroblast Activation Protein (FAP). FAP is a transmembrane protein expressed on fibroblasts and has been shown to have higher expression in idiopathic pulmonary fibrosis (IPF), cirrhosis, and cardiac fibrosis.

NCT ID: NCT05178303 Completed - Clinical trials for Cirrhosis of the Liver

Composition for Treating Cirrhosis and Liver Cancer (SB-1121)

SB-1121
Start date: November 30, 2015
Phase: N/A
Study type: Interventional

The composition treats cirrhosis and hepatocellular carcinoma (Hcc) at an early stage. The product is extracted from herbs, including Adenosma glutinosum extract, Eclipta prostrata extract, Phyllanthus urinaria extract, Impatiens balsamina extract, Ascorbic acid, pyridoxine 5-phosphate, L-Arginine hydrochloride, Pregnenolone acetate. These components have participated in repairing and regenerating new liver parenchyma, preventing fibrosis cell generation, preventing liver cancer cell growth at an early stage. The composition supplements precursors which help the body strengthen antibodies and reduce the risk of inflammation, restore physiological and biochemical functions of liver cells after chronic inflammation.

NCT ID: NCT05170854 Completed - Cirrhosis Clinical Trials

The Impact of Liver Cirrhosis on Outcomes in Trauma Patients

Start date: October 16, 2018
Phase:
Study type: Observational

Given that there are only a few studies on the effects of cirrhosis on trauma patients and none have addressed the impact cirrhosis has on the incidence of infections, it is important that we study this to determine the mortality in cirrhotic trauma patients and ascertain the incidence of infectious complications in these patients. We hypothesize that trauma patients with cirrhosis will have higher rates of mortality and infectious complications.