Hemodynamic Monitoring by FloTrac Sensor in Patients with Acute Congestive Heart Failure

Not Applicable

• Conditions: Acute Congestive Heart Failure

• Registration Number: JPRN-UMIN000019312
• Lead Sponsor: Mitsui Memorial Hospital

Brief Summary

A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-10-14
• Study Completion: 2016-08-10
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

Not provided

Exclusion Criteria

Patients with acute coronary syndrome Patients treated with intra abdominal balloon pump or extracorporeal membrane oxygenation Patients with severe aortic valve regurgitation Patients with atrial fibrilation or flutter Patients who refused enrollment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The correlation between hemodynamic data calculated by FloTrac Sensor (cardiac out put, peripheral vascular resistance, and stroke volume variation) and physical findings, and the correlation between hemodynamic data calculated by FloTrac Sensor and those data calculated by echocardiography.

Secondary Outcome Measures

Name	Time	Method
Short term outcome: in-hospital death, acute renal failure, length of CCU stay, and length of hospital stay. Long term outcome: left ventricular end systolic volume index and brain natriuretic peptide level at 12 months.