Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07643506Phase 1Not yet recruiting
Phase 1, randomised, double-blind trial in postoperative pain comparing 0.9% Saline (Placebo) with 0.5% Bupivacaine group (2 arms). Primary endpoint: Pain intensity numeric rating scale (NRS) at 240 months. Planned start Jun 2026; 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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