Essential Hypertension Clinical Trial
Official title:
Validation of a Hybrid Blood Pressure Monitor to Replace the Mercury Standard for Validation Studies According to Modified Criteria of the European Society of Hypertension International Protocol 2010
Assessment of the accuracy of a Blood Pressure Measuring Device with a digital display-column, NISSEI DM 3000, according to an adaptation of the "European Society of Hypertension International Protocol Revision 2010 for the Validation of Blood Pressure Measuring Devices in Adults".
According to the "European Society of Hypertension International Protocol Revision 2010 for
the Validation of Blood Pressure Measuring Devices in Adults", 33 patients have their blood
pressure measured by two observers using parallel connected mercury sphygmomanometers,
blinded from each other's result, and then by the supervisor using the tested device, NISSEI
DM 3000. The measurements using the mercury sphygmomanometers are repeated 5 times and in
between them, 4 measurements using the tested device take place. If the results of the
comparison of these measurements according to the analysis required by the protocol, meet
the required criteria, the device is regarded as "Pass", otherwise as "Fail".
In this study, instead of consecutive, simultaneous measurements of the two mercury
sphygmomanometers and tha tested device will be taking place. This will be so to exclude any
inaccuracy due to blood pressure variability and because the tested device has a
controllable deflation rate and allows simultaneous measurements with the mercury
sphygmomanometers. In addition, the investigators will be performing 6 set of measurements
instead of 4.
;
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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