About this trial
Spinal anesthesia for elective cesarean section is frequently associated with hemodynamic instability and postoperative complications such as postoperative nausea and vomiting (PONV) and delayed gastrointestinal recovery. Although intraoperative fluid administration is routinely used to prevent spinal-induced hypotension, the optimal fluid strategy remains unclear. Both restrictive and liberal fluid approaches may influence maternal hemodynamics and postoperative outcomes through different physiological mechanisms.
This prospective, single-center, randomized controlled trial aims to compare restrictive (≤3 mL/kg/h) and liberal (\>3 mL/kg/h) intraoperative crystalloid fluid strategies in patients undergoing elective cesarean section under spinal anesthesia. The primary outcome is the incidence of PONV within the first 24 hours postoperatively. Secondary outcomes include postdural puncture headache (PDPH), time to first flatus, hypotension frequency, and vasopressor requirements.
Eligibility criteria
Qualifiers
Female patients aged 18-45 years
ASA physical status II
Scheduled for elective cesarean section under spinal anesthesia
Provision of written informed consent
Disqualifiers
Emergency cesarean section
Preeclampsia or eclampsia
Known cardiac failure
Known renal failure
Trial design
Treatments tested in this trial
- Restrictive intraoperative crystalloid fluid strategy (≤3 mL/kg/h)
- Liberal intraoperative crystalloid fluid strategy (>3 mL/kg/h)