Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07274254Phase 3Recruiting
Phase 3, randomised trial in vaso-occlusive crisis (VOC) comparing Experimental group: Lidocaine + standard of care with Control group: placebo + standard of care (2 arms). Primary endpoint: Cumulative parenteral opioid dose up to 28 days. Started Jul 2026; status: 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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