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Clinical Trial Summary

The goal of this study is to compare the blood pressure control ability with HPI, ClearSight, and conventional NIBP during neuraxial anesthesia in cesarean section. The main question it aims to answer is: Anesthesiologists can have a better control of blood pressure during cesarean section with HPI than with conventional NIBP. During the surgery, the participants will be monitored with standard monitor and HPI with ClearSight and will be randomly assigned to three groups, including HPI group, ClearSight group, and NIBP group. Anesthesiologists will treat intraoperative hypotension with different protocols according to the participants' allocation. Investigators will compare the time-weighted average mean arterial pressure < 65mmHg with in three groups. Secondary outcomes includes the intraoperative hypotension rate, total duration of hypotension, the hypotension symptoms and signs of parturients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05667584
Study type Interventional
Source National Taiwan University Hospital
Contact Po-Yuan Shih, MD
Phone 886-2-23123456
Email shih.poyuan@gmail.com
Status Recruiting
Phase N/A
Start date January 13, 2023
Completion date December 2024

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