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Study To Confirm Efficacy and Safety of Terlipressin in Hepatorenal Syndrome (HRS) Type 1

Hepatorenal Syndrome Clinical Trial

Official title:
A Multi-Center, Randomized, Placebo Controlled, Double-Blind Study to Confirm Efficacy and Safety of Terlipressin in Subjects With Hepatorenal Syndrome Type 1 (The CONFIRM Study)

Clinical Trial Summary

This study is to treat adult patients with hepatorenal syndrome (HRS) Type 1. Out of every three participants, two will receive terlipressin and one will receive placebo. Assignments will be made randomly.

Clinical Trial Description

The primary objective of this trial is to confirm the efficacy and safety of intravenous terlipressin versus placebo in the treatment of adult subjects with hepatorenal syndrome (HRS) Type 1. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02770716
Study type Interventional
Source Mallinckrodt
Contact
Status Completed
Phase Phase 3
Start date July 13, 2016
Completion date July 24, 2019
View Details
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