drugset / Trial / NCT01697410

Summary

The purpose of this study is to evaluate the efficacy of terlipressin for treating septic shock.

Timeline

Start
2013-01
Primary completion
2016-01
Completion
2016-01

Outcome

Missed primary endpoint

paper There was no significant difference in 28-day mortality rate between the terlipressin group (40%) and the NE group (38%) PMID 29971593 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Norepinephrine Other / unclassified 7.5 ug Other
Comparator Norepinephrine Other / unclassified 30 ug Other
Subject Terlipressin Peptide 0.66 ug Other
Subject Terlipressin Peptide 2.66 ug Other