Accuracy evaluation of non-invasive hemodynamic monitor HemoVistaTM (BiLab Co. Ltd. Korea) in the critically ill patients
Not Applicable
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Registration Number
- KCT0008487
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Adult patients aged 20 or older admitted to the surgical intensive care unit of Asan Medical Center in Seoul, who using arterial catheter cardiac output monitoring device at the time of participation.
Exclusion Criteria
Clinically significant arrhythmia (e.g., atrial fibrillation) that may affect the calculation of stroke volume
Patients with cardiac pacemakers or defibrillators
Patients with mechanical circulation aids, such as an extracorporeal oxygen supply (VA-ECMO) or an aortic balloon pump (IABP)
Patients with trauma or skin lesions in the HemoVistaTM sensor attachment (anterior chest)
Any other person deemed inappropriate by researchers
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method cardiac output
- Secondary Outcome Measures
Name Time Method stroke volume variation