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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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NCT ID: NCT03729921 Not yet recruiting - Liver Cirrhosis Clinical Trials

Gastric Variceal Ligation Versus Gastric Variceal Obturation for Secondary Prophylaxis of Gastric Varices

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

The investigators establish a randomized controlled clinical trial, comparing the efficacy and prognosis of GVL and GVO in secondary prevention of GVs, especially in patients with portosystemic shunting, and exploring the endoscopic treatment selection of different types of GVs. Outcome expectations: Compared with glue injection, endoscopic ligation for secondary prevention of gastric varices is safe and effective, especially in patients with portosystemic shunting.

NCT ID: NCT03687216 Not yet recruiting - Clinical trials for Esophageal Varices in Cirrhosis of the Liver

HVPG-Guided Therapy Versus EVL Plus NSBB in Second Prophylaxis of Esophageal Variceal Bleeding

Start date: September 2019
Phase: N/A
Study type: Interventional

A single-center randomized controlled study comparing endoscopic or interventional therapy guided by the hepatic venous pressure gradient (HVPG) , to standard endosopic variceal ligation plus nonselective beta-blocker therapy (NSBB) in patients with esophageal varices due to liver cirrhosis with a history of esophageal variceal hemorrhage.Primary study outcome of the study is variceal rebleeding episodes occurring within the first years after interventions. Second study outcomes of the study are hepatic encephalopathy occurrence, mortality occurrence, liver transplantation or other cirrhosis-related complications.

NCT ID: NCT03675633 Not yet recruiting - Liver Cirrhosis Clinical Trials

Fractional Excretion of Urea for the Differential Diagnosis of Acute Kidney Injury in Liver Cirrhosis

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

The aim of this study is to evaluate the diagnostic performance of FEUrea for the differential diagnosis of AKI in patients with cirrhosis and ascites Specifically, the ability of FEUrea to distinguish between ATN versus Pre renal azotemia and HRS.

NCT ID: NCT03629444 Not yet recruiting - Clinical trials for Sarcopenia in Liver Cirrhosis

Assessment of Sarcopenia in Patients With Liver Cirrhosis and Its Prognostic Value in Liver Transplant Candidates

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

Sarcopenia is a syndrome characterized by progressive and generalized loss of skeletal muscle mass and strength, shown to be prevalent in adults with cancer and common chronic comorbidities such as liver cirrhosis. The EWGSOP identified a grading for Sarcopenia into pre-sarcopenia (decreased muscle mass with normal strength and physical performance), sarcopenia (decreased muscle mass with decreased strength or performance), severe Sarcopenia (decreased muscle mass, strength and performance) . Sarcopenia has emerged as an independent predictor of poor prognosis in a variety of clinical conditions.Sarcopenia is clinically important because it can affectthe quality of life of patients with cirrhosis . Skeletal muscle mass is not only a good indicator of nutrition in patients with cirrhosis, but also has recently been shown to be closely associated with survival prognosis and postoperative complications inHCC. Combination of sarcopenia and the Model for End-stage Liver Disease (MELD) has been shown to be an excellent model for predicting prognosis in decompensated liver cirrhosis . Most patients awaiting liver transplantation (LT) are more or less in a state of sarcopenia. Several studies have reported that sarcopenia was associated with worse prognosis.In addition, sarcopenia may be associated with a higher risk of post-transplant infection . Assessment of sarcopenia in patients with liver cirrhosis:_ The European Working Group on Sarcopenia in Older People recommended that the definition of sarcopenia include not only low muscle mass but also low muscle function . They recommended cutoff values for muscle mass measurements (7.26 kg/m2 for men and 5.5 kg/m2 for women using dual X-ray absorptiometry, and 8.87 kg/m2 for men and 6.42 kg/m2 for women using bioimpedance analysis, handgrip strength (<30 kg for men and <20 kg for women), and usual gait speed (<0.8 m/s). Aim of the study - To evaluate sarcopenia in different stages of liver cirrhosis by different diagnostic methods. - To identify the prognostic value of CT in the diagnosis of sarcopenia . - To identify effect of sarcopenia inliver transplant candidate. Patients and methods: Type of the study:the study is divided into two parts First part: observational descriptive cross sectional study. Second part: follow up of liver transplant candidate group (pre and post liver transplantation) Duration of study: expected duration of the study will be 1.5 years . The 1st part will include all patients admitted to the department for 1 year fulfill inclusion criteria . 2nd part will be 6 ms follow up after liver transplantation. Study population 1. st part : Patients with liver cirrhosis will be evaluated for the presence of sarcopenia. 2. nd part: - 13 cases of liver cirrhosis already done liver transplantation in AL Rajhiuneversitiy hospital(which data already recoreded) and any cirrhotic pts will be prerared for liver transplantion within six months. - Methods At the study entry, all candidates will be subjected to the following parameters (and 3 month after LT for liver transplant candidates only) - Clinical history - Clinical examination - Abdominal ultrasound - Laboratory investigation: - Liver function tests - Complete blood picture, - Kidney function tests, - Serum glucose, serum Na+ and K+ - Hepatitis markers (HBsAg, HCV-Ab) - Calculate: = Child Pugh score (Pugh et al., 1973) and MELD (Wiesner et al., 2003) scores for assessment ofliver cirrhosis. - Anthropometric measurements: - Triceps skin fold thickness (TSF) . - Measure mid-arm circumference (MAC). - Body mass index - Hand grip to assess muscle strength - Gait speed to assess physical performance - Assessment of sarcopenia using CT scan: - Assessment of sarcopenia using ultrasound: - Assessment of sarcopenia using bioimpedance analysis

NCT ID: NCT03623360 Not yet recruiting - Liver Cirrhosis Clinical Trials

Functional MRI to Determine Severity of Cirrhosis

Start date: September 2018
Phase:
Study type: Observational

This is a pilot study to investigate the feasibility of a novel MRI technique to assess the severity of liver cirrhosis and predict complications based on functionality and perfusion measurements whilst maintaining image quality. The principal objective of this pilot study is to assess liver function and the future risk of complications in patients with cirrhosis, using novel techniques and measures based on free-breathing Dynamic Contrast Enhanced MRI. Specifically the investigators will assess: 1. Whether sufficient data can be generated in patients with cirrhosis whilst maintaining image quality, and 2. The dynamic range of DCE-MRI measures in patients with cirrhosis. This pilot study will, if successful, provide sufficient data to support applications for larger studies to evaluate the clinical utility of a DCE-MRI imaging biomarker in patients with cirrhosis.

NCT ID: NCT03580577 Not yet recruiting - Liver Cirrhosis Clinical Trials

Risk Factors and Outcomes of Acute Venous Thromboembolism in Cirrhotic

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

patient with liver cirrhosis was supposed to have autoanticoagulation which approved to be wrong, with absence of conventional method to detect all abnormalities in coagulation state. Thromboelastography (TEG) give a broad picture for the coagulation defects. In addition to that no guidelines prescribed anticoagulants for venous thromboembolism in cirrhotic, so the investigators will do a study to demonstrate frequency and risk factors for acute venous thromboembolism in cirrhotic patients, find a conventional laboratory method and test TEG to assess risk of thrombosis in cirrhotic patients.Also, to validate current algorithm for use of anticoagulant and antiplatelet for thromboembolism for non cirrhotic in cirrhotic patients.

NCT ID: NCT03529136 Not yet recruiting - Clinical trials for Decompensated Liver Cirrhosis

Clinical Trial of Umbilical Cord Mesenchymal Stem Cell Transfusion in Decompensated Liver Cirrhosis

Start date: June 1, 2018
Phase: Phase 2
Study type: Interventional

Decompensated liver cirrhosis is one of the life-threatening complication of chronic liver disease. Liver transplantation currently is the only effective method that can improve the survival of these patients. However, the severe shortage of donor livers, high cost, and potential serious complications have restricted the availability of liver transplantation.Umbilical cord mesenchymal stem cells (UC-MSC) has been generally shown to be safe and effective for liver diseases in some pre-clinical and clinical studies. This study aim to evaluate the safety and efficiency of human umbilical cord mesenchymal stem cell transfusion in patients with decompensated liver cirrhosis, and explore the best protocol of MSC transfusion.

NCT ID: NCT03492879 Not yet recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

Non Invasive Electrical Impedance Technology (EIT) for Diagnosing Liver Diseases Severity

Start date: May 15, 2018
Phase: N/A
Study type: Interventional

The aims of this study are to assess the performance of the non-invasive Electrical Impedance Technology (EIT) in evaluating the liver fibrosis stage in patients with chronic liver diseases, in comparisons with a liver biopsy and/or Shear wave elastography and Liver Ultrasonography. The second aim is comparing between Liver Ultrasonography and Electrical Impedance Technology (EIT) to quantify the hepatic steatosis grade in patients with Non Alcoholic Fatty Liver Disease (NAFLD) .

NCT ID: NCT03487159 Not yet recruiting - Liver Diseases Clinical Trials

Using the Non Invasive Technology Magnetic Resonance Elastography for the Diagnosis of Liver Fibrosis Stage

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This study evaluates the ability of Magnetic Resonance Elastography non invasive technology to identify the liver fibrosis stage in patients with chronic liver diseases compared to Shear Wave Elastography and/or Liver Biopsy.

NCT ID: NCT03482076 Not yet recruiting - Liver Cirrhosis Clinical Trials

Iron Deficiency Anemia in Childern With Liver Cirrhosis

IDA
Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Iron deficiency anemia is a common complication of liver cirrhosis in childern and may affects there life this study to improve the outcome of these patients