FindTrial
Sign In

Data collection study using a chest worn wearable device on Healthy subjects

A single centre, open, non-controlled, observational, investigator initiated, data collection study on healthy subjects using an investigative non-invasive chest worn wearable device - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/101284
Enrollment
1000
Registered
2026-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

None listed

Interventions

Intervention1: Nil: Nil

Sponsors

Anusar Medequips Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age above 40 years 2.Patients having enough cognitive ability to give informed consent

Exclusion criteria

Exclusion criteria: 1.Having symptoms of severe dehydration such as extreme drowsiness and weak pulse 2.Having symptoms of fluid overload such as shortness of breath, pedal edema or raised JVP 3.Pregnant women 4.Having any implanted devices such as pacemakers, ICDs etc. 5.Suffering from cancer, severe liver disease or sepsis 6.Having previous history of heart failure related hospital admissions 7.Having end stage renal disease

Design outcomes

Primary

MeasureTime frame
Deriving the normal range of fluid score across gender, height, weight, BMI and chest circumferenceTimepoint: At baseline only—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactSriram Ganesan

Anusar Medequips Pvt Ltd

sganesan@anusar.com9845396992

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026