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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT02056041 Completed - Cirrhosis Clinical Trials

Selection Criteria for Safe Hepatectomy for Hepatocellular Carcinoma

Start date: January 2004
Phase: N/A
Study type: Observational

Selection criteria for safe hepatectomy for HCC are not well established. The aim of this study was the validation of the selection criteria for safe hepatectomy for hepatocellular carcinoma.

NCT ID: NCT02026609 Terminated - Cirrhosis Clinical Trials

Glutamine Challenge as Predictor of Hepatic Encephalopathy After Transjugular Intrahepatic Portosystemic Shunt (TIPS)

Start date: May 2013
Phase: N/A
Study type: Observational

Transjugular intrahepatic portosystemic shunt (TIPS) is the first-line therapy for patients with cirrhosis and refractory ascites. However, mental changes known as hepatic encephalopathy (HE) frequently occur after TIPS. There is no effective method to predict HE after TIPS. Oral glutamine challenge (OGC) and psychometric tests have been used to assess the risk for HE, but never in patients undergoing TIPS. Severe muscle loss may also predispose patients to HE. The aim of the present study is to assess if both the OGC and psychometric tests can accurately predict the development of overt HE after TIPS. Patients will be studied before TIPS and followed after TIPS for the development of HE. The role of muscle loss in favoring HE, as well as is possible reversibility after TIPS will also be investigated.

NCT ID: NCT02017119 Completed - Cirrhosis Clinical Trials

Comparison Between Lactulose and Lactulose-Paraffin in Cirrhotic Patients

Start date: January 2011
Phase: Phase 2
Study type: Interventional

Hepatic encephalopathy (HE) is an important complication of liver cirrhosis. Lactulose is a first line treatment for HE, but the adherence to this treatment is relatively low, due to side effects such as diarrhea, distention, etc.

NCT ID: NCT02016196 Completed - Cirrhosis Clinical Trials

Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS

PRPET
Start date: September 2013
Phase: Phase 3
Study type: Interventional

TIPS has been used for 20 years, as a means of reducing portal pressure in patients with cirrhosis and portal hypertension related complications. TIPS proved more effective than alternative treatments in controlling or preventing variceal bleeding and refractory ascites. The main drawback of the TIPS procedure is progressive overt hepatic encephalopathy (OHE). Three risk factors for post-TIPS OHE have been identified: age over 65 years, history of previous episodes of OHE, and Child-Pugh score equal to or over 10. However, the incidence of post-TIPS OHE in patients fulfilling these criteria remains close to 35 %.

NCT ID: NCT02009748 Completed - Clinical trials for Vitamin D Deficiency

Vitamin D Supplementation in Cirrhotic Patients

Start date: December 2013
Phase: Phase 2
Study type: Interventional

Previous studies suggested that vitamin D deficiency is highly prevalent in cirrhotic patients and is related to the degree of liver dysfunction as well as mortality. In gastrointestinal disorders, vitamin D absorption can be highly reduced. We herein aim to investigate the efficacy of oral vitamin D supplementation in cirrhotic patients with vitamin D insufficiency.

NCT ID: NCT01992978 Recruiting - Clinical trials for Hepatocellular Carcinoma

Radiofrequency-assisted Hepatectomy on the Outcomes of HCC Patients With Cirrhosis

Start date: November 2013
Phase: N/A
Study type: Interventional

Surgical resection is the most effective treatment of primary and secondary liver tumors. Technical innovations have mainly focused on minimizing bleeding during transection of the hepatic parenchyma because excessive hemorrhage and the need for blood transfusion are associated with increased postoperative morbidity and mortality. Recently,radiofrequency-assisted(RFA)hepatectomy has developed rapidly and gained widespread acceptance for the treatment of hepatocellular carcinomas(HCC),but its influence on the prognosis of HCC patients,especially for those with cirrhosis,is still controversial. Therefore, we design this prospective clinical trial to explore the effect of RFA hepatectomy versus the conventional hepatectomy on the outcomes of perioperative period and prognosis of HCC patients with cirrhosis.

NCT ID: NCT01987791 Unknown status - Hepatitis B Clinical Trials

Observation Study of Prednisone and Cyclosporine in Treatment of Thrombocytopenia in Hepatitis B Cirrhosis

Start date: January 2005
Phase: N/A
Study type: Observational

To compare the safety and efficacy of 12 months of low dose prednisone with low dose cyclosporine combined with entecavir in patients with thrombocytopenia associated with HBV-related cirrhosis.

NCT ID: NCT01960127 Completed - Cirrhosis Clinical Trials

Effects of Aerobic Training on Exercise Capacity in Patients With Advanced Cirrhosis 2

Start date: October 15, 2013
Phase: N/A
Study type: Interventional

Cirrhosis is associated with a reduction in muscle mass and exercise capacity. This has an impact on morbidity and mortality. Regular aerobic exercise training is a proven effective therapy to improve exercise capacity in healthy and clinical populations. The effect of this training has not yet been evaluated in the decompensated cirrhosis patient population. The safety of this intervention also requires further study. Using a randomized controlled design, the investigators aim to determine the safety and efficacy of eight weeks of aerobic exercise training on aerobic capacity, functional performance, and muscle mass in decompensated cirrhosis patients.

NCT ID: NCT01956864 Withdrawn - Clinical trials for Hepatocellular Carcinoma

Study of High-Dose Oral Vitamin D for the Prevention of Liver Cancer

Start date: September 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of a high dose of vitamin D (VD) in patients with cirrhosis. The investigator hypothesizes that high dose VD will be safe and well-tolerated in adults with cirrhosis, and will inhibit the inflammatory and proliferative events that cause progression of cirrhosis to hepatocellular carcinoma.

NCT ID: NCT01954524 Terminated - Cirrhosis Clinical Trials

A Phase 1, Open-Label Study of Intravenous Sildenafil in Patients With Cirrhosis

Start date: May 2014
Phase: Phase 1
Study type: Interventional

Safety and tolerability of a single dose intravenous bolus injection of Sildenafil in patients with moderate to severe cirrhosis and kidney disease will be determined.