Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2024-513688-25-01Phase 4Authorised
Phase 4, randomised, double-blind trial in postoperative pain comparing PENG block with ropivacaine with PENG block with saline placebo (2 arms). Primary endpoint: Area under curve (AUC) of pain on NRS 0–10 in first 24 hours postoperatively. Planned start Jun 2024; status: authorised.
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.
See how Gosset can support your research on 2024-513688-25-01.