Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06683807Not yet recruiting
Randomised, double-blind trial of bupivacaine in cesarean section (2 arms), sponsored by Assiut University. Primary endpoint: Incidence of post-dural puncture headache at 120 hours. Planned start Dec 2024; status: not yet recruiting.
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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