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Comparing a wearable patch s vital sign readings with standard hospital devices in patients.

CLINICAL EVALUATION OF A NON INVASIVE WEARABLE DEVICE FOR MULTI PARAMETER HEALTH MONITORING AND PREDICTIVE ANALYSIS - SUSHENA-Vitals Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/12/098729
Enrollment
120
Registered
2025-12-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: Z69-Z76- Persons encountering health services in other circumstances

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil Intervention5: Nil: Nil Intervention6: Nil: Nil

Sponsors

Sriram R, Vitritya Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants will be enrolled across the following age categories Infants (1 month to 24 months) Paediatric population (24 months to 17 years) Adults (18 to 75 years) All participants must be medically stable, free from any severe chronic illness, and suitable for non-invasive vital sign monitoring.

Exclusion criteria

Exclusion criteria: Individuals with implantable medical devices or pregnancy will be excluded.

Design outcomes

Primary

MeasureTime frame
Agreement between device and clinical standardsTimepoint: Multiple Time points during the hospital stay—

Secondary

MeasureTime frame
To assess patient and clinician feedback on comfort, safety, and usabilityTimepoint: at the end of data collection process—

Countries

India

Contacts

Public ContactDrJayaraj Mymbilly Balakrishnan

Kasturba Medical College , MAHE , Manipal

jayaraj.mb@manipal.edu9895063580

Outcome results

None listed

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