Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04653506Completed
Randomised, double-blind trial in Postpartum pain (PPP) comparing Paracetamol group with Ibuprofen group (2 arms). Primary endpoint: Pain relief (NRS) at 6 hours. Started Nov 2020; 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.
See how Gosset can support your research on NCT04653506.