Apply to trial NCT07661758

A few quick questions so the study team can decide if you might be a fit.

RecruitingPhase 3Drug trial

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

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.

How this works

Answer a few questions
About 5 to 10 minutes. Skip-friendly where possible.
We connect you with the study team
When a site picks up your application, we introduce you to their team directly — with you on the thread.
The team reaches out to schedule screening
Usually within a few business days, via the contact you give.

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

How this works

Answer a few questions

We connect you with the study team

The team reaches out to schedule screening