Noninvasive Continuous Blood Pressure Monitoring for Cesarean Delivery

Noninvasive Continuous Blood Pressure Monitoring for Preventing Post-spinal Hypotension During Cesarean Delivery: A Randomized Controlled Trial

Noninvasive continuous blood pressure monitoring for preventing post-spinal hypotension during cesarean delivery: A randomized controlled trial

The aim of this study was to find out whether the incidence of hypotension during surgery can be reduced in the case of non-invasive, continuous blood pressure monitoring using the ClearSight System in patients undergoing cesarean section under spinal anesthesia, compared to the case of using conventional noninvasive blood pressure monitoring

Inclusion Criteria:

• Adult mothers who are pregnant with single fetuses over 35 weeks gestational age undergoing planned cesarean delivery under spinal anesthesia

Exclusion Criteria:

• Multiple fetal pregnancy

  • Preexisting hypertension or pregnancy-induced hypertension

    • Underlying heart disease

      • Underlying cerebrovascular disease

        • Known fetal anomaly

          • Contraindicated in spinal anesthesia

            • Any sign of onset of labor

              • Body weight <45 kg or body weight> 90 kg

                • Height <145cm or height> 180cm

                  • All other cases in which researchers determine to be inappropriate for this clinical trial