Hemodynamics Clinical Trial
Official title:
Validation and Comparison of Ballistocardiographic Biosensors and Other Hemodynamic Measures for Healthy Subjects During Different Situations
Ballistocardiographic (BCG) biosensors reflecting the patients' current state is established.
There are few studies documenting BCG biosensors efficacy, effectiveness, and efficiency. In
addition, technologies using invasive blood pressure curves and Near Infrared Regional
Spectrometry (NIRS) to measure hemodynamics have been used. Using these technologies to guide
clinical decisions may be an major advance for patients with acute and chronic diseases. The
investigators will explore how these technologies compares to well established technologies
measuring vital signs of healthy subjects. The investigators will use live continuous and
non-continuous biosensor data to monitor the development of vital parameters during different
scenarios. The study will document how CPD measured by biosensors, cerebral oximetry measured
by NIRS, and invasive blood pressure curves measured by FloTracâ„¢ are compared to established
technologies of vital organ functionality.
Data will be measured continuously and documented simultanuously with technologies such as
Doppler Echocardiography, transthoracic impedance (TTI), Electrocardiogram (ECG), invasive
blood pressure [cardiac output/index (CO/CI), stroke volume/stroke volume index (SV/SVI),
stroke volume variation/pulse pressure variation (SVV/PPV), systemic vascular resistance/
systemic vascular resistance index (SVR/SVRI), mean arterial pressure (MAP)], pulse oximetry
(SpO2) and cerebral oximetry (rSO2). Of special interest is to document how relative heart
stroke volume reflects blood flow documented by the parallel technology measures. All these
measures are the key part in the study to document user friendliness, accuracy, sensitivity,
specificity and correlations.
The main research question is whether adding BCG biosensor measures, cerebral oximetry and
invasive blood pressure to monitor vital signs will add meaningful information to the care of
patients in a situation where we are able to control all the factors that may impact these
measures. The aim of the study is to document (correlation, sensitivity and specificity) how
BCG biosensors perform compared to each other and to well established technologies used for
monitoring blood flow, blood pressure, heart rate and respiration rate in steady state and
during ambulance transport. In addition, the investigators will in a controlled manner
measure how established maneuvers like Trendelenburg, hypo-/hyperventilation, and bolus of
fluid influences our measures.
Ballistocardiographic (BCG) biosensors collecting continuous physiological data (CPD) in real
time to generate information reflecting the patients' current state is established and have
become more useful in monitoring vital signs of subjects and patients. There are few studies
documenting BCG biosensors efficacy, effectiveness, and efficiency. Using CPD to guide
clinical decisions may be a major advance for patients with acute and chronic diseases. In
addition, technologies using invasive blood pressure curves and Near Infrared Regional
Spectrometry (NIRS) to measure hemodynamics have been used. This may drive the evolution from
episodic to continuous patient care for these patients experiencing a severe medical event
compromising blood flow. The investigators will explore how these technologies compares to
well established technologies measuring vital signs of healthy subjects. In the present study
the investigators will use live continuous and non-continuous biosensor data to monitor the
development of vital parameters during different scenarios. The study will document how CPD
measured by biosensors, cerebral oximetry measured by NIRS, and invasive blood pressure
curves measured by FloTracTM are compared to established technologies of vital organ
functionality.
In the present study data will be measured continuously and in phases of the study
simultaneously with other well established technologies such as Doppler Echocardiography,
transthoracic impedance (TTI), Electrocardiogram (ECG), invasive blood pressure [cardiac
output/index (CO/CI), stroke volume/stroke volume index (SV/SVI), stroke volume
variation/pulse pressure variation (SVV/PPV), systemic vascular resistance/ systemic vascular
resistance index (SVR/SVRI), mean arterial pressure (MAP)], pulse oximetry (SpO2) and
cerebral oximetry (rSO2). Based on this the investigators believe they will be able to pick
up how dynamic differences develop. Of special interest is to document how relative heart
stroke volume reflects blood flow documented by the parallel technology measures. HRV will
also be evaluated in the light of other measures such as pulse, respiration, and relative
stroke volume. All these measures are the key part in the study to document user
friendliness, accuracy, sensitivity, specificity and correlations.
The main research question is whether adding BCG biosensor measures, cerebral oximetry and
invasive blood pressure to monitor vital signs will add meaningful information to the care of
patients in a situation where we are able to control all the factors that may impact these
measures. The aim of the study is to document (correlation, sensitivity and specificity) how
BCG biosensors perform compared to each other and to well established technologies used for
monitoring blood flow, blood pressure, heart rate and respiration rate in steady state and
during ambulance transport. In addition, the investigators will in a controlled manner
measure how established maneuvers like Trendelenburg, hypo-/hyperventilation, and bolus of
fluid influences our measures.
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