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Portal Hypertension clinical trials

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NCT ID: NCT01440829 Completed - Portal Hypertension Clinical Trials

The Effectiveness of L-ornithine-L-aspartate (LOLA) on Plasma Ammonia in Cirrhotic Patients After TIPS

Start date: December 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the effectiveness of L-ornithine-L-aspartate (LOLA) on plasma ammonia in cirrhotic patients after Transjugular Intrahepatic Portosystemic Shunt (TIPS) procedure.

NCT ID: NCT01410591 Completed - Portal Hypertension Clinical Trials

TIPS With 8- OR 10-mm Covered Stent for Preventing Variceal Rebleeding

T8/10SVB
Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether transjugular intrahepatic portosystemic shunt (TIPS) with 10-mm covered stent is associated with lower shunt dysfunction in comparing TIPS with 8-mm covered stent in cirrhotic patients with at least one episode of variceal bleeding.

NCT ID: NCT01408966 Completed - Cirrhosis Clinical Trials

Effects of Dark vs. White Chocolate on the Postprandial Increase in Portal Pressure in Cirrhosis

Start date: August 2008
Phase: Phase 2
Study type: Interventional

This study was aimed at testing the hypothesis that supplementing a meal with dark chocolate, which holds potent antioxidant properties, might attenuate the postprandial increase in the hepatic venous pressure gradient (HVPG, clinical equivalent of portal pressure) in patients with cirrhosis

NCT ID: NCT01358123 Recruiting - Liver Cirrhosis Clinical Trials

Value of Von Willebrand Factor in Portal Hypertension

Start date: September 2006
Phase: N/A
Study type: Observational

In patients with liver cirrhosis elevated levels of von Willebrand factor antigen (vWF-Ag) are found frequently but the clinical significance is unclear. vWF-Ag plays an important role in primary haemostasis and development of thrombotic vascular obliteration is discussed as a possible mechanism leading to portal hypertension. Invasive measurement of hepatic venous pressure gradient (HVPG) is the current gold standard for the diagnosis of portal hypertension. The investigators hypothesize that vWF-Ag levels in plasma may correlate with portal pressure and predict clinically significant portal hypertension (CSPH, HVPG >=10mmHg) and its complications.

NCT ID: NCT01282398 Not yet recruiting - Liver Cirrhosis Clinical Trials

Study About Simvastatin in Portal Hypertension in Compensated Cirrhosis

SIMPRO
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether simvastatin is effective in the prevention of progression of porta hypertension in compensated cirrhosis patients.

NCT ID: NCT01282385 Not yet recruiting - Liver Cirrhosis Clinical Trials

Hemodynamic Effect of Simvastatin With Beta Blockers in Clinical Portal Hypertension

SIMBETA
Start date: April 2011
Phase: Phase 4
Study type: Interventional

In the genesis and maintenance of PH associated with liver cirrhosis are two mechanisms that act synergistically. The first is an increase in hepatic vascular resistance, due in part to the disruption of liver structure inherent cirrhosis, and increased hepatic vascular tone is caused by the contraction of perivascular smooth muscle cells, myofibroblasts and hepatic stellate cells, which represents about 30% of global intrahepatic resistance and is believed to be due to the production Defective nitric oxide (NO). The second mechanism, which maintains and exacerbates HTP, is an increase of splanchnic blood flow caused by increased NO and other vasodilators at this level In this regard, we believe that in patients with compensated liver cirrhosis, with portal pressure gradient> 10 mmHg, both acute responders betablockers test as non-responders, the association of antifibrotic drugs and / or vasodilators, chronic liver selective May be beneficial in the control of portal hypertension

NCT ID: NCT01267669 Completed - Cirrhosis Clinical Trials

A Trial of Somatostatin With Endoscopic Variceal Ligation (EVL) in Control of Acute Variceal Bleeding

AVB-EVL+S
Start date: November 2005
Phase: N/A
Study type: Interventional

Background: Efficacy of endoscopic variceal sclerotherapy in achieving initial control of acute variceal bleeding and five-day haemostasis has been shown to significantly improve when vasoactive drug is added. However, there is limited data whether addition of somatostatin, to endoscopic variceal ligation (EVL) improves the efficacy of EVL. Aim: To compare EVL plus somatostatin versus EVL plus placebo in control of acute variceal bleeding. Patients and methods: Consecutive cirrhotic patients with acute variceal bleeding from esophageal varices were enrolled in the trial. After emergency EVL, patients were randomized to receive either somatostatin (250 mcg/hr) or placebo infusion. Primary endpoint was treatment failure within 5 days. Treatment failure was defined as fresh hematemesis ≥2 hour after start of therapy or death.

NCT ID: NCT01236339 Terminated - Liver Cirrhosis Clinical Trials

Early TIPS for Ascites Study

Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that TIPS with the GORE® VIATORR® TIPS Endoprosthesis improves transplant-free survival compared to LVP alone in patients who have cirrhosis of the liver with portal hypertension and difficult to treat ascites.

NCT ID: NCT01188733 Completed - Cirrhosis Clinical Trials

Efficacy of Long-acting Octreotide (Sandostatin LAR) in Reducing Portal Pressure in Patients With Cirrhosis

Start date: June 1998
Phase: Phase 1/Phase 2
Study type: Interventional

Octreotide is used to control variceal bleeding. However, octreotide has to be given through the vein and is effective for less than two hours. In this study the investigators determined whether a long-acting preparation of octreotide (Sandostatin LAR)given as an intra-muscular injection every month could decrease portal pressure, and thus be used to prevent variceal bleeding in patients with cirrhosis.

NCT ID: NCT01131962 Completed - Portal Hypertension Clinical Trials

Comparing Two Methods to Stop Vomiting of Blood Using the Endoscope

Start date: May 2008
Phase: Phase 3
Study type: Interventional

Band ligation and injection sclerotherapy are two modalities of treatment that are applied using the endoscope. The purpose of this study is to determine which of two methods is better for controlling bleeding from the upper gut.