Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07838909Completed
Randomised, double-blind trial in Post-operative cognitive dysfunction (POCD) comparing Group Ketamine, Group Lidocaine and Group Placebo (3 arms). Primary endpoint: Incidence of postoperative cognitive dysfunction at 3 days. Started Mar 2025; 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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