Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05596227Completed
Randomised, double-blind trial (3 arms), sponsored by Tanta University. Primary endpoint: Total postoperative fentanyl requirements at 24 hours. Started Oct 2022; 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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