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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT00163995 Recruiting - Cirrhosis Clinical Trials

Urotensin II and Vascular Tone in Cirrhosis

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

This study looks at the iontophoresis of urotensin II in chronic liver disease patients.

NCT ID: NCT00162552 Completed - Cirrhosis Clinical Trials

Clinical Trial of Pentoxifylline in Patient With Cirrhosis

PENTOCIR
Start date: August 2004
Phase: Phase 3
Study type: Interventional

In patients with cirrhosis and liver failure, pro-inflammatory cytokines (TNF alpha) might be responsible of severe complications and death. Thus, the prevention of cytokine production should prevent complications and mortality. The aim of this study is to study the 2 months survival rate in patients with severe cirrhosis (Child-Pugh C) with pentoxifylline - an inhibitor of cytokine production. The 6 month mortality, the proportion of transplanted patients, the occurrence of complications (bacterial infection, renal failure, hepatic encephalopathy and gastrointestinal bleeding), plasma cytokine levels and fibrotest - a marker of fibrosis - will be also studied. This is a multicenter double blind randomized trial with a placebo. All adult patients with severe cirrhosis might be randomized after written consent. Patients with severe carcinoma, intolerance or contraindication to pentoxifylline will not be included. Patients receive either pentoxifylline or placebo 3 times a day for 6 months. Three hundred and forty two patients are necessary to decrease mortality rate by 50% at 2 months in a beta risk of 10% and an alpha risk of 5%. Patients will be seen every month.

NCT ID: NCT00154492 Completed - Cirrhosis Clinical Trials

Use of NovoSeven® in Active Variceal Bleeding

Start date: April 2004
Phase: Phase 2
Study type: Interventional

This trial is conducted in Asia and Europe. The trial is planned to investigate the effectiveness and safety of NovoSeven® in patients with advanced cirrhosis and active variceal bleeding.

NCT ID: NCT00151671 Terminated - Clinical trials for Hepatocellular Carcinoma

Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer

IMPACT
Start date: April 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Cirrhotic patients undergoing hepatic resection have a mortality rate near 10%, and 30 to 70% of them develop severe complications. These failures are mainly due to hepatic insufficiency. Studies have already shown benefits of oral nutritional supplements in ORL, digestive, and cardiac surgery. We aimed to ascertain whether this nutritional, immune-enhancing supplementation, administered 7 days before and 3 days after surgery, could improve liver function and postoperative host defences in patients with liver cancer resection.

NCT ID: NCT00125762 Completed - Hepatitis C Clinical Trials

FibroScan in Patients With Hepatitis B and C Presenting for Liver Biopsy

Start date: March 2005
Phase: N/A
Study type: Interventional

This study will examine the effectiveness of the FibroScan device in differentiating fibrosis in patients with hepatitis B and C. The FibroScan measures liver stiffness and will be correlated to the liver biopsy to see if it can diagnose the stage of liver disease. Patients who are scheduled to have a liver biopsy will also have a fibroscan and the stiffness will be correlated with the biopsy stage.

NCT ID: NCT00124228 Completed - Cirrhosis Clinical Trials

Albumin Administration in Patients With Cirrhosis and Infections Unrelated to Spontaneous Bacterial Peritonitis

Infecir
Start date: November 2004
Phase: Phase 3
Study type: Interventional

Spontaneous bacterial peritonitis (SBP) present in cirrhotic patients induces severe circulatory dysfunction, which results in renal failure in up to 30% of the patients. Renal failure is an important prognostic marker, representing the major predictive factor of in-hospital mortality. Recent studies have shown that plasma volume expansion with albumin associated with cefotaxime in patients with SBP is more efficient to prevent renal failure than cefotaxime treatment alone. The in-hospital and three-month mortality rates, furthermore, were significantly lower in the group treated with albumin. It is not known if other bacterial infections unrelated to SBP represent a risk factor for the development of renal failure among cirrhotic patients. The researcher's group has recently performed a study to evaluate the incidence, characteristics and outcome, of renal failure in patients with cirrhosis and bacterial infections unrelated to SBP associated with the systemic inflammatory response syndrome (Terra, unpublished results). Among a total of 106 patients, 29 (27%) presented renal failure during the course of infection. Renal failure was characterized by intense renal vasoconstriction (intrarenal resistive index of 0.83 +/- 0.09, measured by Doppler ultrasound), reduction of mean arterial pressure and an important activation of endogenous vasoconstriction systems. The three-month survival probability of patients with infection and renal failure was 34 %, much lower than that of patients with infection but not presenting renal failure (87%, p<0.0001). These results suggest that the development of renal failure in patients with cirrhosis and bacterial infections different from SBP, associated with signs of a systemic inflammatory response, is very frequent and results in a very poor prognosis. Taken as a whole, these data strongly indicate the need to consider these patients as candidates for liver transplantation and to plan strategies for its prevention. The objective of this project, therefore, is to evaluate if the plasma volume expansion with albumin, associated with conventional antibiotic therapy, can prevent the development of renal failure and increase survival rates in cirrhotic patients with bacterial infections unrelated to spontaneous bacterial peritonitis.

NCT ID: NCT00122135 Completed - Lung Cancer Clinical Trials

A Culturally Sensitive Values-Guided Aid for End of Life Decision-Making

Aim3
Start date: December 2004
Phase: N/A
Study type: Interventional

The goal of this research agenda is to improve the quality of end-of-life care by explicitly identifying values that will guide the decision-making process, with a particular emphasis on the role of ethnic, racial and cultural factors.

NCT ID: NCT00115947 Completed - Cirrhosis Clinical Trials

Renal and Cardiovascular Effects of Terlipressin in Patients With Cirrhosis and Ascites

Start date: December 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect of terlipressin on myocardial perfusion and renal function. Hypothesis: Significant improvement of renal function reflected by: glomerular filtration rate (GFR), renal blood flow (RBF), excretion of salt and metabolites in the urine and related hormones and peptides in the blood. No effect on the systolic function of the heart.

NCT ID: NCT00108355 Completed - Cirrhosis Clinical Trials

Vasoconstrictors as Alternatives to Albumin After Large-Volume Paracentesis (LVP) in Cirrhosis

Start date: December 2003
Phase: Phase 4
Study type: Interventional

This clinical trial compares a combination of two drugs that constrict blood vessels (Octreotide LAR and Midodrine) to albumin after large volume paracentesis. Subjects have cirrhosis and ascites.

NCT ID: NCT00096733 Completed - Clinical trials for Hepatocellular Carcinoma

Adult-to-Adult Living Donor Liver Transplantation Study

A2ALL-1
Start date: October 2004
Phase: N/A
Study type: Observational

There are two principal purposes of this study: 1) to determine whether it is more beneficial for a liver transplant recipient candidate to pursue a living donor liver transplant (LDLT) or wait for a deceased donor liver transplant (DDLT), and 2) to study the impact of liver donation on the donor's health and quality of life.