Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2008-003566-26Phase 4Completed
Phase 4, randomised, open-label trial in postoperative pain comparing Intravenous oxycodone then oral oxycodone/naloxone with Piritramide infusion (2 arms). Primary endpoint: Pain intensity 3 hours after first study medication intake. Started Sep 2008; 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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