drugset / Trial / NCT00279214

Hemodynamic and Perfusion Response to Drotrecogin Alfa (Activated) in Patients With Septic Shock

NCT00279214 ↗

Phase 4 Completed 43 enrolled Eli Lilly and Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The study will evaluate the vasopressor requirement, hemodynamic response and measures of tissue perfusion in patients with septic shock receiving an infusion of drotrecogin alfa (activated) compared to patients not receiving drotrecogin alfa (activated).

Timeline

Start
2005-11
Primary completion
—
Completion
2007-11

Outcome

Missed primary endpoint

registry analysis (superiority or other test); Drotrecogin Cohort vs Control Cohort; p = 0.238; Repeated Measures - propensity adjusted NCT00279214 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Drotrecogin alfa (activated) Protein / enzyme biologic — Other