Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02783586Phase 4Completed
Phase 4, randomised, double-blind trial of bupivacaine in postoperative pain, sponsored by Medical University of Warsaw. Primary endpoint: Total postoperative fentanyl usage at 24 hours. Started Apr 2016; 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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