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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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NCT ID: NCT02778425 Completed - Portal Hypertension Clinical Trials

The Treatment of Hepatocirrhosis and Portal Hypertension

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

This study compare the efficiency of partial splenic embolization +endoscopical therapy with endoscopical therapy alone in gastroesophageal variceal haemorrhage accompanied with splenomegaly or hypersplenism of hepatocirrhosis and portal hypertension treatment.

NCT ID: NCT02767206 Enrolling by invitation - Liver Cirrhosis Clinical Trials

Evaluation of Gastroesophageal Varices by Transnasal Endoscopy.

Start date: March 2016
Phase: N/A
Study type: Observational

The study aims to evaluate the feasibility of transnasal endoscopy in patients with portal hypertension, cirrhotic and non-cirrhotic. The incidence of the procedure's adverse effects, the patient's tolerance and his/her opinion about the exam are analyzed. In addition, the interobserver matched for the discoveries found in the study is carried out.

NCT ID: NCT02752529 Recruiting - Cirrhosis, Liver Clinical Trials

The Establishment of Multiple Point Prediction Model About Tacrolimus Metabolic Differences Based on Genetic Network After Liver Transplantation and the Application of Multicenter

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

Combined with the clinical data of FK506 and the database of GO and Kyoto Encyclopedia of Genes and Genomes(KEGG), the investigators aim to carry out the bioinformatic analysis and build a muti-locus genetic model, then muti-center assess the predictive accuracy of FK506 metabolic differences.

NCT ID: NCT02744105 Completed - Clinical trials for Beta Thalassemia Major

Effect of Spirulina on Liver Fibrosis by Transient Elastography in Beta Thalassemic Children With Hepatitis C

Start date: December 2015
Phase: N/A
Study type: Interventional

Thalassemics can develop liver fibrosis because of iron overload and hepatitis C infection. The latter is the main risk factor for liver fibrosis in transfusion dependent thalassemics. Excess liver iron is clearly recognized as a co factor for the development of advanced fibrosis in patients with hepatitis virus C infection. Transient elastography (Fibroscan) is a reliable non invasive method for diagnosing as liver fibrosis in thalassemic patients regardless of the degree of iron overload. There is evidence that suggests Spirulina may help to protect against liver damage, cirrhosis and liver failure in those with chronic liver disease.

NCT ID: NCT02739581 Withdrawn - Advanced Cirrhosis Clinical Trials

Efficacy and Safety of Endoscopic Variceal Ligation (EVL) Versus EVL Plus Non-selective B-blockers (NSBB) For Prevention of Variceal Rebleed and Non-bleed Related Complications in Patients With Advanced Cirrhosis

Start date: n/a
Phase: N/A
Study type: Interventional

The patients will be randomized into two groups 1. Endoscopic Variceal Ligation with Non Selective Beta Blocker 2. Placebo with Endoscopic Variceal Ligation

NCT ID: NCT02732405 Not yet recruiting - Hepatitis C Clinical Trials

Study to Investigate Tolerability and Efficacy of MK5172 / MK8742 Without Ribavirin for 12 Weeks in Patients With Chronic HCV G1b Infection With Compensated Cirrhosis

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

To assess efficacy (SVR rate) of MK5172 / MK8742 for 12 weeks without RBV in G1b patients with compensated cirrhosis (Child-Pugh A5 to A6) previously failing first gen. PI or non responders to PR.

NCT ID: NCT02710227 Not yet recruiting - Liver Cirrhosis Clinical Trials

Sleep Timing and Circadian Preferences in A Sample of Egyptian Patients With Hepatic Cirrhosis

Start date: September 2018
Phase: N/A
Study type: Observational

Individuals with hepatic cirrhosis (n=50) and healthy controls (n=30) were recruited. Sleep quality, sleep timing parameters and circadian preference were evaluated using the Pittsburgh Sleep Quality Index (PSQI), Sleep Timing Questionnaire (STQ) and The Composite Scale for Morningness (CSM) respectively

NCT ID: NCT02705742 Recruiting - Liver Cirrhosis Clinical Trials

Mesenchymal Stem Cells Transplantation for Liver Cirrhosis Due to HCV Hepatitis

Start date: January 2016
Phase: Phase 1/Phase 2
Study type: Interventional

In this study, investigators aimed to transplant autologous, adipose tissue derived mesenchymal stem cells to the patients with liver cirrhosis due to HCV. We also aimed to assess liver tissue regeneration, downgrade of clinical findings and antiviral efficacy. Finally investigators aimed to establish an alternative treatment modality to liver transplantation.

NCT ID: NCT02705534 Completed - Hepatitis C Clinical Trials

Sofosbuvir, Ledipasvir, Ribavirin for Hepatitis C Cirrhotics, Genotype 1

SL50
Start date: September 2016
Phase: Phase 3
Study type: Interventional

The investigators will treat 50 patients with cirrhosis due to hepatitis C genotype 1, with sofosbuvir 400 mg daily, ledipasvir 90 mg daily and weight-based ribavirin (1000 mg/d if <75 kg, 1200 mg/d if >75 kg, divided in two daily doses) for 12 weeks and calculate the sustained viral response rate at 12 weeks.

NCT ID: NCT02702739 Completed - Liver Cirrhosis Clinical Trials

Sofosbuvir/Simeprevir Plus a Flat Dose of Ribavirin in Genotype 1 Elderly HCV Cirrhotic Patients

HCV
Start date: January 2015
Phase: Phase 4
Study type: Interventional

The proportion of HCV infected patients over age 65 years in Western countries is increasing. This growth and the advent of new antiviral therapy bring into the question the real world efficacy and safety of the combination of Sofosbuvir and Simeprevir (SOF/SMV) plus a flat dose of ribavirin (RBV) in elderly patients compared to younger patients.