Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00571636Phase 3Completed
Phase 3, randomised, double-blind trial in pain comparing Fentanyl Continuous Infusion with Placebo Continuous Infusion (2 arms). Primary endpoints: Premature Infant Pain Profile at 7 days and Echelle Douleur Inconfort Nouveau-Nè at 7 days. Started Dec 2007; 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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