Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2025-522462-73-00Phase 4Authorised
Phase 4, randomised, double-blind trial in anesthesia complication comparing Perioperative intravenous lidocaine with Perioperative intravenous placebo (sodium chloride) (2 arms). Primary endpoint: Composite postoperative opioid-related adverse events within 48 hours. Planned start Mar 2026; status: authorised.
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.
See how Gosset can support your research on 2025-522462-73-00.