Satavaptan in the Prevention of Ascites Recurrence in Patients With Ascites Due to Cirrhosis of the Liver

• Status: Terminated
• Trial end date: 2008-10-01
• Target enrollment: 0
• Participant gender: All

Summary

Primary To evaluate the efficacy of satavaptan on top of diuretic drugs in reducing the recurrence of ascites.

Secondary To evaluate the tolerability and safety of satavaptan on top of diuretic drugs over a 52-week treatment period in participants with cirrhosis of the liver and recurrent ascites.

The one-year double blind placebo controlled period is extended up to 2 years in a long term safety study (PASCCAL-2).

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Sanofi
• Treatments: Satavaptan

Criteria

Inclusion Criteria:

• Participants with cirrhosis of the liver.

• Participants with recurrent ascites having undergone both of the following:

• therapeutic paracentesis for the removal of ascites in the previous 24 hours with the removal of > 4 litres of fluid.

• at least one other therapeutic paracentesis in the previous 3 months.

Exclusion Criteria:

• Participants with an existing functional transjugular intrahepatic portosystemic shunt (TIPS) or other shunt.

• Known hepatocellular carcinoma.

• Participants with ascites of cardiac origin or due to peritoneal infection (e.g. tuberculosis) or peritoneal carcinoma.

• Participants previously exposed to satavaptan in the past 12 months.