Congestive Heart Failure Clinical Trial
Official title:
Validation of Measurements From CoVa Sensor (VALIDATION-CO-1) Study to Assess Measurements of Wireless Cardiac Output Device
Heart failure is a common cardiovascular problem which is increasing in both prevalence and incidence and associated with substantial morbidity and mortality. The management of heart failure patients is complex and has become a priority world over. Effective methods to keep heart failure patients out of the hospital are essential, both in the interests of the patient's health, as well as to reduce the burden on the health care system
Heart failure patients should be in a position to provide readings of their weight, blood
pressure, fluid intake, thoracic fluid, heart rate, heart rate variability, respiration
rate, stroke volume, cardiac output, medications and other important parameters and
communicate this data to care providers using wireless technology. This data should be made
available to medical personnel regularly and on a periodic basis. In this manner the health
care providers can detect and respond to warning signs or alerts before the patient's
condition worsens to warrant a visit to the doctor or a hospital admission with features of
heart failure decompensation. Programs for chronic heart failure that include remote
monitoring have been shown to have a positive effect on clinical outcomes in community
dwelling patients with chronic heart failure.
In preparation for a study evaluating the effectiveness of mobile monitoring, the value of
Stroke Volume and Cardiac Output need to be validated against FDA approved devices that are
available in a hospital or clinic setting. This study covers the validation of the
measurements taken with the proposed home monitoring device, Perminova's CoVaTM Sensor
(Sensor) against clinic devices such as bio-impedance devices, echocardiogram, Doppler
and/or MRI
;
Observational Model: Cohort, Time Perspective: Prospective
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