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A Clinical Study in Adults to evalute the Accuracy and Safety of a Non-Invasive Chair-Based Device for Measuring Vital Signs

Accuracy, Performance and Safety Evaluation of the AHC Device for Non-Invasive Physiological Measurements: A Prospective Clinical Investigation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104623
Enrollment
110
Registered
2026-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: Z000- Encounter for general adult medical examination

Interventions

Intervention1: Nil: Nil

Sponsors

Aarogya Tech, Inc
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged greater than 18 years Male or female subjects Able and willing to provide written informed consent Able to comply with study procedures Patient must be able to sit comfortably in the chair

Exclusion criteria

Exclusion criteria: Pregnant or breastfeeding women Pediatric subjects less than 18 years Inability to comply with procedures Any condition deemed unsuitable by the Investigator Patient difficult to sit in the chair

Design outcomes

Primary

MeasureTime frame
Accuracy metrics such as mean bias, limits of agreement, mean absolute error, and repeatability for each physiological parameter compared with reference devices.Timepoint: Single study visit (during device measurements).

Secondary

MeasureTime frame
Secondary Endpoints include incidence and nature of safety events and Subject-reported discomfort or difficulties during device use, if applicableTimepoint: Throughout the study visit until completion of all measurements.

Countries

India

Contacts

Public ContactDr SA Dilipan

Apollo Speciality Hospital, Vanagaram

dilipan_sa@yahoo.co.in9884455766

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026