Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06369948Completed
Randomised, double-blind trial of bupivacaine in postoperative pain (2 arms), sponsored by Fayoum University Hospital. Primary endpoint: Total opioid consumption post operative at 48 hours. Started Mar 2024; status: completed.
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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