Validation Study of CONTEC08C Electronic Sphygmomanometer
Trial Parameters
Brief Summary
The purpose of this study is to assess the accuracy of the CONTEC08C automated oscillometric upper-arm sphygmomanometer in the general population for clinical use according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension /International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018).
Eligibility Criteria
Inclusion Criteria: * Subjects aged 12 to 79 years * Subjects voluntarily participate in the clinical trial and sign the informed consent. Exclusion Criteria: * Subjects with cardiac arrhythmias; * Pregnancy; * Poor quality Korotkoff sounds; * Subject with an arm injury incompatible with the use of a cuff-based sphygmomanometer; * Other conditions that the investigator considers ineligible for clinical trial.