Body Impedance Method in Patients Undergoing Urgent and Elective Cesarian Section

• Conditions: Cesarean Section Complications

• Registration Number: NCT04230525
• Lead Sponsor: Gaziosmanpasa Research and Education Hospital

Brief Summary

Independent form anesthetic methods, during C/S, considering both maternal and fetal conditions, some crucial hemodynamic changes can appear and can be claimed non invasively with the whole body bioimpedance. In this research, any kind of hemodynamic difference between this method and urgent or elective C/S case will be detected and the clinic pursuit can be developed creating an advantage in favor of both maternal and fetal conditions.

Detailed Description

Independent form anesthetic methods, during C/S, considering both maternal and fetal conditions, some crucial hemodynamic changes can appear and can be claimed non invasively with the whole body bioimpedance. In this research, any kind of hemodynamic difference between this method and urgent or elective C/S case will be detected and the clinic pursuit can be developed creating an advantage in favor of both maternal and fetal conditions. Under general anesthesia, measuring the hemodynamic changes with the method of non-invasive whole-body bioimpedance system during C/S.

Detection of in which phase of operations the potential changes densify and differences between urgent and elective conditions non invasively.

Study Timeline

• Study First Submitted: 2020-01-13
• Study First Submitted QC: 2020-01-13
• Study First Posted: 2020-01-18
• Study Start: 2020-03-05
• Status Verified: 2020-06
• Primary Completion: 2020-06-05
• Last Update Submitted: 2021-03-04
• Last Update Posted: 2021-03-08
• Study Completion: 2021-06-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 95

Inclusion Criteria

• Must be scheduled for elective or emergency cesarean section

Exclusion Criteria

• History of cardiac surgery, and advanced cardiac valvular disease

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
MAP	1, 5, 15, and 30 minutes following the induction of the anesthesia	The difference in mean arterial pressure during the cesarean section between elective and emergency ceasreansection subjects

Trial Locations

Locations (1)

Gaziosmanpaşa TREH; 🇹🇷 Istanbul, Gaziosmanpaşa, Turkey