An open label, non-invasive single centric study to validate710_Blood Pressure Monitor machine for standard use
Not Applicable
- Registration Number
- CTRI/2024/07/070168
- Lead Sponsor
- eInfoChips Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Able to provide written informed consent prior to participation in the
study.
Exclusion Criteria
Special populations, presence of any arrhythmia and any issues
during the validation procedure. Excluded subjects must be reported
with reasons for exclusion.
If K1 or K5 is not audible
Unable or unwilling to provide written informed consent.
Patients are not eligible to provide blood pressure in the opinion of the investigator.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Accuracy of blood pressure measurement compared with the mercury sphygmomanometer and <br/ ><br>Omron (If applicable).Timepoint: 10 Blood pressure reading to be taken within 30 mins
- Secondary Outcome Measures
Name Time Method Differences between the tested device & the mercury sphygmomanometer & Omron deviceTimepoint: 30 mins