Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07012889Not yet recruiting
Randomised, double-blind trial in postoperative pain comparing The lidocaine group with The placebo group (2 arms). Primary endpoint: Opioid consumption during the first 24 hours after the surgery. Planned start Jun 2025; status: not yet recruiting.
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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