Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00521703Phase 3Completed
Phase 3, randomised, double-blind trial of lidocaine in dyspepsia, malabsorption syndrome, gastroesophageal reflux disease (GERD) and 1 more, sponsored by Hospital Infantil Cândido Fontoura. Primary endpoint: propofol dose required to achieve adequate sedation at 1 hour. Started Aug 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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