Evaluation of Clinical Utility of Non-invasive Hemodynamic Monitoring Device

Recruiting

• Conditions: Cardiovascular Complication

• Registration Number: NCT05996965
• Lead Sponsor: Seoul National University Hospital

Brief Summary

In patients undergoing surgery under general anesthesia, the clinical utility of non-invasive hemodynamic status monitoring equipment using HemoVista is compared with invasive hemodynamic status monitoring equipment FloTrac.

Detailed Description

For patients who are scheduled to monitor invasive blood pressure, invasive hemodynamic monitoring using FloTrac and additional HemoVista sensors are attached and output data are obtained at the same time during general anesthesia. FloTrac is used to conduct conventional anesthesia and fluid therapy, and the accuracy of HemoVista, a non-invasive hemodynamic monitoring equipment, is compared through prospective observational studies.

Study Timeline

• Study First Submitted: 2023-08-10
• Study First Submitted QC: 2023-08-10
• Study First Posted: 2023-08-18
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-20
• Study Start: 2023-11-21
• Last Update Posted: 2023-11-22
• Primary Completion: 2024-12-10
• Study Completion: 2024-12-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Adult patients aged 20 or older who undergo surgery under general anesthesia for more than two hours
• invasive close hemodynamic monitoring with FloTrac is needed

Exclusion Criteria

• problems in site where HemoVista is attached

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
degree of agreement in cardiac output	during surgery	degree of agreement in cardiac output between HemoVista and FloTrac

Trial Locations

Locations (1)

Hee-Soo Kim; 🇰🇷 Seoul, Soul-t'ukpyolsi, Korea, Republic of