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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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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: NCT03269877 Not yet recruiting - Hypersplenism Clinical Trials

Hypersplenism in Patients With Liver Cirrhosis and Portal Hypertension

Start date: September 1, 2017
Phase: N/A
Study type: Observational

The spleen could be considered a neglected organ. To date, it has been deemed an ancillary organ in portal hypertension or an organ localization in lymphoproliferative diseases. Hypersplenism is a common disorder characterized by an enlarged spleen which causes rapid and premature destruction of blood cells. It can result from any splenomegaly. It is most common with splenomegaly secondary to portal hypertension and hematological disorders. Portal Hypertension is an important cause of splenomegaly in most tropical countries This work will involve a series of studies aiming to: 1. Assess the prevalence and pattern of hypersplenism, and grade the severity of cytopenias in patients with cirrhosis and portal hypertension. 2. Elucidate the relationship between hypersplenism, in these patients, and: 1. The severity of liver cirrhosis as assessed by Child's and the Model of End-stage Liver Disease (MELD) scores. 2. The presence and grade of gastroesophageal varices as assessed by upper endoscopy. 3. The presence of hepatocellular carcinoma 4. Portal hemodynamics and portal vein thrombosis as assessed by Doppler Ultrasound. 3. Test the hypothesis that leucopenia in cirrhotic patients may be caused, at least in part, by apoptosis of polymorphnuclear leucocytes.

NCT ID: NCT03269786 Not yet recruiting - Liver Cirrhosis Clinical Trials

Changes in Lab and Ultrasonography After Endoscopic Varisceal Treatment

Start date: November 1, 2018
Phase:
Study type: Observational

laboratory and ultrasongraphicc changes after endoscopical varices treatment

NCT ID: NCT03267615 Recruiting - Liver Cirrhosis Clinical Trials

VICIS - Vienna Cirrhosis Study

VICIS
Start date: February 1, 2017
Phase:
Study type: Observational [Patient Registry]

Patients with advanced chronic liver diseases treated at the Vienna General Hospital of the Medical University of Vienna will be offered to participate in this prospective observational trial. Clinical parameters and laboratory parameters will be recorded for all patients and patients will undergo a regular follow-up schedule with clinical visits at the Vienna General Hospital. This study is linked to a biobank with serum/plasma, ascitic fluid, urine, GI tract mucosal biopsies, liver biopsies and stool collected from the study participants.

NCT ID: NCT03265249 Terminated - Pain, Postoperative Clinical Trials

BRIDGE Device for Post-operative Pain Control

BRIDGE
Start date: February 12, 2018
Phase: N/A
Study type: Interventional

Auricular neurostimulation is a potential novel and non-invasive method of pain control following liver transplantation in a growing patient population with the probability of significant impact on economics and morbidity. The investigators propose a pilot study to investigate the effects of auricular neurostimulation in patients receiving a liver transplantation. The investigator will investigate the effects of auricular neurostimulation with this novel device and compare it to the current standard of care for pain management following liver transplantation.

NCT ID: NCT03263598 Completed - Liver Cirrhosis Clinical Trials

Validation of Diagnostic Usefulness of the Random Urine Na/K Ratio for Replacement of 24hr Urine Na Excretion in Cirrhotic Patients With Ascites

urine Na/K
Start date: May 2016
Phase:
Study type: Observational [Patient Registry]

The low sodium intake is important for ascites control in liver cirrhosis patients. Therefore, World Health Organization (WHO) recommends reduction of sodium (Na) to 2g/day for adults. The 24-hour urine Na excretion has been regarded as a standard method to estimate the amount of daily dietary sodium intake. However, it is too inconvenient to apply to patients or the general population in practice. For this reason, it has been suggested that a spot urine Na/potassium (K) ratio could be replaced with the 24-hour urine Na excretion. However, the evidence is not sufficient for that. The investigators will evaluate the usefulness of spot urine Na/K ratio to estimate the dietary sodium intake. The investigators will also verify several formulas of estimating the 24-hour Na excretion with spot urine Na, K, Creatinine (Cr).

NCT ID: NCT03254758 Completed - Clinical trials for Decompensated Liver Cirrhosis

A Study of ADR-001 in Patients With Liver Cirrhosis

Start date: July 20, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This is a first-in-human Phase1/2 study of ADR-001, adipose-derived mesenchymal stem cells (AD-MSCs). The safety and preliminary efficacy are evaluated in Phase 1 in patients with liver cirrhosis caused by Hepatitis C or Nonalcoholic Steatohepatitis and a recommended Phase 2 dose is determined by the evaluation. The exploratory efficacy and safety are investigated against the same target population in Phase 2.

NCT ID: NCT03245606 Completed - Clinical trials for Non-Alcoholic Fatty Liver Disease

Combining MRI Steatosis Assessment and Transient Elastography to Improve Liver Fibrosis Diagnosis in Non Alcoholic Fatty Liver Disease

FibroMR
Start date: December 7, 2017
Phase:
Study type: Observational

The main objective is to compare the accuracy of transient elastography taking into account liver steatosis determined by MRI, to liver biopsy for the diagnosis of liver fibrosis ≥F2 in patient with NAFLD.

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: NCT03241823 Not yet recruiting - Hepatitis C Clinical Trials

Assessment of Patients With Hepatitis C Virus Related Liver Cirrhosis After Sustained Response to Direct Acting Anti Viral Drugs.

Start date: December 1, 2017
Phase: N/A
Study type: Observational

Hepatitis C Virus (HCV) infection is a major global health challenge; it is estimated that more than 80 million people are chronically infected worldwide, with 3-4 million new infections and 350,000 deaths occurring each year because of HCV-related complications .