Clinical Trial

Intravenous Lidocaine to Prevent Post-Fundal Pressure Headache During Cesarean Section

Study acronym: LID-HEAD
Recruiting Phase 3
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Summary
This prospective randomized controlled multicenter study will be conducted to evaluate the effects of pre-emptive IV lidocaine dose on the incidence and severity of intraoperative headache that may occur after the extra-abdominal manual uterine fundal pressure in patients undergoing cesarean section under spinal anesthesia.
Protocol Amendment History 1 change
critical Recruitment opened 2026-07-07
Trial Details
NCT Number NCT07661758
Lead Sponsor Tanta University
Conditions Intravenous Lidocaine, Fundal Pressure, Headache
Enrollment 680 participants
Start Date 2026-07-01
Primary Completion 2026-11-01 (estimated)
Study Completion 2026-11-02 (estimated)
Updated on ClinicalTrials.gov 2026-07-06