Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05004506Phase 3Unknown
Phase 3, randomised, single-blind trial of bupivacaine in postoperative pain (2 arms), sponsored by Loyola University Chicago. Primary endpoints: Analgesic efficacy (VAS scores) at 48 hours, Rescue narcotics use and 1 more. Status: unknown.
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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