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Observational study on 50 admitted heart failure patients for congestion level assessment using an investigative chest-worn wearable device

A non invasive chest worn wearable device in assessing congestion levels in acutely decompensated heart failure patients An Observational Pilot - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/092786
Enrollment
50
Registered
2025-08-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: I504- Combined systolic (congestive) anddiastolic (congestive) heart failure

Interventions

Intervention1: Nil: Nil

Sponsors

Anusar Medequips Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age above 18 years 2.Patients under diuretic treatment for heart failure 3.Patients having enough cognitive ability to give informed consent

Exclusion criteria

Exclusion criteria: 1.Pregnant women or women planning for pregnancy 2.Having any implanted devices such as pacemakers, ICDs etc. 3.Suffering from cancer 4.Suffering from severe liver disease or in septic shock

Design outcomes

Primary

MeasureTime frame
Correlation and statistical analysis of device reported fluid scores with current state of the art clinical methods (NTproBNP, fluid balance and Echocardiogram reported RVSP)Timepoint: At baseline (time of admission), at the time of discharge (typically 2 to 7 days), at the time of OPD visit (typically 7 days after discharge—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactSriram Ganesan

Anusar Medequips Pvt Ltd

sriram.ganesan@anusar.ai9845396992

Outcome results

None listed

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