Clinical Trials Directory

Trials / Unknown

UnknownNCT03485833

End-expiratory and End-inspiratory Occlusion Tests to Predict Fluid Responsiveness

End-expiratory and End-inspiratory Occlusion Tests to Predict Fluid Responsiveness in Mechanically Ventilated Cardiac Surgical Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Shanghai Zhongshan Hospital · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to verify the efficacy of using end-expiratory and end-inspiratory occlusion tests as an index of fluid responsiveness in mechanically ventilated patients with cardiac surgery.

Detailed description

Patients with hypotension after anesthetic induction for cardiac surgery, who requires fluid resuscitation based on clinical judgement by the anesthesiologists are enrolled in this study. Patients are monitored by transesophageal echocardiography and FloTrac/Vigileo. Hemodynamic variables (heart rate, systolic blood pressure, diastolic blood pressure, mean artery pressure, central venous pressure, stroke volume variation, cardiac index, velocity time integral of the aorta etc) are measured at baseline, after end-expiratory occlusion (EEO) test, after end-inspiratory occlusion (EIO) test, after passive legs raising test, and after fluid challenge respectively. Responders are defined by an increase in velocity time integral over 15% after infusion of 5ml/kg of crystalloid solution.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTEEO and EIO testvelocity time integral of the aorta measured by transesophageal echocardiography after end-expiratory and end-inspiratory occlusion test

Timeline

Start date
2018-01-01
Primary completion
2020-12-31
Completion
2020-12-31
First posted
2018-04-02
Last updated
2018-04-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03485833. Inclusion in this directory is not an endorsement.