Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2008-000504-92Phase 3Terminated
Phase 3, randomised, double-blind trial in Vasoplegia and septic shock comparing PHP plus conventional vasopressor therapy with Placebo plus conventional vasopressor therapy (2 arms). Primary endpoint: 28-day all-cause mortality. Started Oct 2008; status: terminated.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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