drugset / Trial / NCT00592475

A Study to Assess the Safety and Effects of Intravenous (IV) Conivaptan on the Hepatic Hemodynamic Response in Cirrhotic Patients

NCT00592475

Phase 2 Completed 20 enrolled Cumberland Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the safety of IV conivaptan in stable euvolemic or hypervolemic cirrhotic patients, and to characterize the effects of IV conivaptan on the hepatic hemodynamic response in patients with cirrhosis.

Timeline

Start
2007-12
Primary completion
2008-11
Completion
2008-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Conivaptan Small molecule 2.5 mg Intravenous
Subject Conivaptan Small molecule 5 mg Intravenous

Indications