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Monitoring Patients With Acute Cardiac Disease Using a Wireless, Wearable, Non-invasive Monitor

B

Biobeat

Status

Completed

Conditions

Acute Cardiac Pulmonary Edema
Acute Cardiac Failure
Acute Cardiac Event

Treatments

Device: Non-invasive Monitoring

Study type

Observational

Funder types

Industry

Identifiers

NCT04635371
PPGCICUWOMC

Details and patient eligibility

About

A prospective observational study in patients admitted with an acute cardiac disease, in which the PPG-based device will be attached to them on admission, for frequent monitoring of their vitals during hospitalization and interventional procedures. in parallel to currently-used and approved devices. Data will be crossed with gathered clinical and laboratory data, to study the device's ability to detect acute hemodynamic and respiratory changes during hospitalization, and gathering workflow information from the nursing staff.

Enrollment

70 patients

Sex

All

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men and women aged 18 years and above admitted to the Cardiac ICU due to an acute cardiac event.

Exclusion criteria

  • Pregnant women, subjects under the age of 18 years.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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