Actively Recruiting
Validation Study of CONTEC08C Electronic Sphygmomanometer
Led by Chinese Academy of Medical Sciences, Fuwai Hospital · Updated on 2024-06-24
100
Participants Needed
1
Research Sites
9 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
Validation Study of CONTEC08C Electronic Sphygmomanometer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects aged 12 to 79 years
- Subjects voluntarily participate in the clinical trial and sign the informed consent.
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chinese Academy of Medical Sciences，Fuwai Hospital
Beijing, Beijing Municipality, China, 100037
Actively Recruiting
Research Team
Y
Ying Lou, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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