Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05076435Phase 2Completed
Phase 2, randomised, open-label trial in sepsis (2 arms). Primary endpoint: 24-hour intravenous crystalloid fluid administration. Started Nov 2021; status: completed.
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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