Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2016-001486-90Phase 3Completed
Phase 3, randomised, double-blind trial in respiratory distress syndrome (RDS) and neonatal complications of very preterm birth comparing Standard-dose betamethasone with Reduced-dose betamethasone (50% dose) + placebo (2 arms). Primary endpoint: Severe respiratory distress syndrome (RDS). Started Apr 2016; 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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