KCT0008487
Not Yet Recruiting
N/A
Accuracy evaluation of non-invasive hemodynamic monitor HemoVistaTM (BiLab Co. Ltd. Korea) in the critically ill patients: A prospective observational study
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Sponsor
- Asan Medical Center
- Enrollment
- 20
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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