Clinical Trials Directory

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UnknownNCT03139929

Measurement of MSFP and Stressed Volume With CardioQ+®

Measurement of Mean Systemic Filling Pressure & Stressed Volume With CardioQ+® Oesophageal Doppler Measurement

Status
Unknown
Phase
Study type
Observational
Enrollment
42 (estimated)
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To study the reliablity of MSFP and stressed volume to follow volume loading and to predict fload loading responsiveness in patients after elective coronary artery bypass grafting (CABG) surgery.

Detailed description

In this study the oesophageal Doppler monitor (CardioQ+), arterial pulse wave analysis (via the CardioQ+ and Flotrac device) and central venous pressure (CVP) will be used to estimate mean systemic filling pressure (MSFP) with the inspiratory hold method. Furthermore the MSFParm will be determined using a rapid cuff inflator. From MSFP vascular compliance (Csys) and stressed volume (Vs) will be calculated. The accuracy of Vs to follow a 500 increase in volume will be studied. The accuracy of MSFP and Vs to to predict fluid loading responsiveness will be assessed in 42 patients after elective coronary artery bypass grafting (CABG) surgery. The effect of a standardised fluid loading on parameters of intrinsic contractility and afterload will be determined. The effect of fluid loading on inertia, resistance and elastance will be assessed

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTMSFPMSFPhold and MSFParm

Timeline

Start date
2017-05-09
Primary completion
2019-05-05
Completion
2020-03-01
First posted
2017-05-04
Last updated
2020-01-13

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT03139929. Inclusion in this directory is not an endorsement.