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Study identifier: NCT07661758 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Intravenous Lidocaine · Fundal Pressure · Headache  ·  Sponsor: Tanta University

PhasePhase 3
Planned participants680
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Osama M Rehab, MD  ·  +201095210806  ·  osamarehab@med.tanta.edu.eg

Always discuss trial participation with your own doctor first.

Locations (1)

Tanta University HospitalsTanta, Gharbia Governorate, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07661758