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An open label, non-invasive single centric study to validate 710_Blood Pressure Monitor machine for standard use

An open label, non-invasive single centric study to validate 710_Blood Pressure Monitor POC in adult population - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/07/070168
Enrollment
100
Registered
2024-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Control Intervention1: NIL: NIL

Sponsors

eInfoChips Private Limited
Lead Sponsor
Fervor Health Solutions Private limited
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Able to provide written informed consent prior to participation in the study.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Accuracy of blood pressure measurement compared with the mercury sphygmomanometer and Omron (If applicable).Timepoint: 10 Blood pressure reading to be taken within 30 mins—

Secondary

MeasureTime frame
Differences between the tested device & the mercury sphygmomanometer & Omron deviceTimepoint: 30 mins—

Countries

India

Contacts

Public ContactSharad Jain

Fervor health solutions

sharad@fervorhs.com8527110300

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026