drugset / Trial / NCT00089570

Study of Terlipressin Versus Placebo to Treat Hepatorenal Syndrome Type 1

NCT00089570 ↗

Phase 3 Completed 112 enrolled Mallinckrodt
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether terlipressin is safe and effective in the treatment of patients with hepatorenal syndrome (HRS) type 1 when compared to placebo.

Timeline

Start
2004-06
Primary completion
2006-03
Completion
2006-09

Outcome

Missed primary endpoint

paper Treatment success with terlipressin was double that with placebo (25% vs 12.5%, P = .093). PMID 18471513 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Terlipressin Peptide 1 mg Intravenous
Subject Terlipressin Peptide 2 mg Intravenous

Indications