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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT00741663 Completed - Cirrhosis Clinical Trials

Spironolactone Versus Spironolactone Plus Furosemide (SVSSF)

SVSSF
Start date: April 2005
Phase: Phase 4
Study type: Interventional

The question whether the sequential diuretic therapy, that means using an antialdosteronic drug at first and adding a loop diuretic in nonresponders, is better than the combination of the two diuretics from the beginning (combined diuretic therapy) in the treatment of ascites in patients with cirrhosis is still open. Therefore, the aim of the study is to compare sequential versus combined diuretic therapy in these patients. One hundred patients will be randomized into two groups. Group A will receive potassium canrenoate at the initial dose of 200 mg/day, then increased up to 400 mg/day. Non responders will be treated with 400 mg/day of potassium canrenoate and furosemide at an initial dose of 50 mg/day, then increased up to 150 mg/day. Group B will receive at first 200 mg/day of potassium canrenoate and 50 mg/day of furosemide, then increased up to 400 mg/day and 150 mg/day, respectively. The percentage of responders to dthe diuretic treatment, the time to get the resolution of ascites and the rate of adverse effects will be compared between the two Groups of Patients.

NCT ID: NCT00713934 Completed - Cirrhosis Clinical Trials

Autologous Bone Marrow Stem Cells in Cirrhosis Patients

Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Liver cirrhosis (LC) is the end stage of chronic liver disease. The liver transplantation is one of the only effective therapies available to such patients. However, lack of donors, surgical complications, rejection, and high cost are it`s serious problems. The potential for stem cells in bone marrow (BM) to differentiate into hepatocytes cells was recently confirmed. Moreover, BMC transplantation has been performed to treat hematological diseases, and several clinical studies have applied BMC injection to induce regeneration of myocardium and blood vessels. In this study we will evaluate safety and feasibility of autologous bone marrow mono nuclear (BM-MNC) and enriched CD133+ hematopoietic stem cell transplantation through the portal vein in patients with decompensate cirrhosis.

NCT ID: NCT00701792 Completed - Cirrhosis Clinical Trials

Liver Transplantation Versus Alternative Therapies for Patients With Pugh B Alcoholic Cirrhosis

TRANSCIAL
Start date: March 1994
Phase: N/A
Study type: Interventional

Liver transplantation has been universally recognized to improve survival of patients suffering from end-stage (Pugh C) alcoholic cirrhosis. However, for Pugh B patients, the benefit of liver transplantation remains to be demonstrated. The aim of the present study was to compare the outcome of Pugh B patients with alcoholic cirrhosis randomly assigned for immediate liver transplantation (group 1) or standard treatments (group 2).

NCT ID: NCT00629421 Completed - Clinical trials for Hepatocellular Carcinoma

Early Screening of Hepatocellular Carcinoma in Cirrhotic Patients: a Prospective Study

Start date: January 1, 2001
Phase: N/A
Study type: Observational

Although serum alpha-fetoprotein level and abdominal sonography are the main methods to screening hepatocellular carcinoma (HCC) in cirrhotic patients, the adequate time and methods used are not completely well-defined. This study aims to assess the better timing and methods for prospectively screening HCC in patients with cirrhosis

NCT ID: NCT00603200 Withdrawn - Fatigue Clinical Trials

Effect of Large Volume Paracentesis on Fatigue in Cirrhosis

Start date: January 2008
Phase:
Study type: Observational

The purposeof this study is to determine the effect of a large volume paracentesis (procedure in whihc a catheter is placed to remove fluid from the abdomen) on the severity of fatigue i patients with cirrhosis (severe scarring of the liver) and large volume ascites (fluid in the abdomen).

NCT ID: NCT00596414 Completed - Anxiety Clinical Trials

Sedation and Analgesia for Transjugular Liver Biopsy: A Randomized Double Blind Placebo Controlled Trial

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

Transjugular liver catheterisation allows the measurement of hepatic venous pressure gradient (HVPG) and the sampling of liver tissue but patient's tolerance to the procedure is unknown. The aim of this study was to assess tolerance to transjugular hepatic liver biopsy with or without conscious sedation/analgesia.

NCT ID: NCT00594191 Completed - Cirrhosis Clinical Trials

Efficacy and Safety of Simvastatin in the Treatment of Portal Hypertension

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

The purpose of this study is to evaluate the effects of continuous simvastatin administration on the hepatic venous pressure gradient (HVPG), as a surrogate marker of prognosis, and its safety in patients with cirrhosis and portal hypertension.

NCT ID: NCT00570973 Completed - Cirrhosis Clinical Trials

Band Ligation Versus Transjugular Intrahepatic Portosystemic Stent Shunt (TIPS) in Cirrhotics With Recurrent Variceal Bleeding Non Responding to Medical Therapy

ENDOvsTIPS
Start date: November 2004
Phase: Phase 4
Study type: Interventional

Patients with liver cirrhoses and recent history of variceal bleeding, with HVPG documented non response to medical therapy with non selective beta blockers +/- mononitrates or variceal rebleeding during adequate medical therapy will be randomized to undergo either multi-session endoscopic multi-band ligation and continuation of medication or TIPS placement. Best treatment for this group of cirrhotic patients is not known so far.

NCT ID: NCT00570622 Completed - Cirrhosis Clinical Trials

Effect of Pioglitazone on Portal and Systemic Hemodynamics in Patients With Advanced Cirrhosis

Start date: December 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the response to pioglitazone on the hepatic venous pressure gradient and peripheral vascular responsiveness to vasoconstrictors in patients with advanced (Child´s Grade B or C) cirrhosis.

NCT ID: NCT00534677 Completed - Cirrhosis Clinical Trials

The Safety & Efficacy of Terlipressin vs Octreotide for the Control of Variceal Bleed

Start date: May 2004
Phase: Phase 4
Study type: Interventional

Terlipressin and Octreotide are two common agents used as adjuvants in the management of variceal bleeding. Both agents have been claimed equivalent to endoscopic therapy in randomized studies. There are no head to head clinical trials of these two agents available in the literature. We aimed to compare the efficacy and safety of Terlipressin and Octreotide in combination with Endoscopic Variceal band Ligation (EVL)in patients presenting with Esophageal Variceal Bleed (EVB).