Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03053947Phase 2Completed
Phase 2, open-label, single-arm trial of ketamine in laceration. Primary endpoints: Optimal dose of intranasal ketamine for adequate procedural sedation at 18 months and Evaluation of the dose determined in DosINK 1 at 18 months. Started Feb 2017; 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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