Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04104204Unknown
Randomised, double-blind trial of bupivacaine in postoperative pain (2 arms), sponsored by Mahidol University. Primary endpoint: Time to first analgesic request (PCA fentanyl) at 48 hours. 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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