Advanced Wireless, Wearable Sensors for Continuous Hemodynamic Monitoring

Northwestern University

Status: Completed

Conditions: Congestive Heart Failure

Treatments: Device: wearable vital signs sensor

Study type: Observational

Funder types: Other

Identifiers

NCT04362553

STU00210413

Details and patient eligibility

About

Percent agreement of vital signs monitoring between the experimental sensor and standard of care monitoring

Enrollment: 42 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

1. Patient's aged 18-65
2. Patient's scheduled to undergo a Trans-thoracic Echocardiogram (TTE) in an outpatient cardiology clinic or admitted to the Cardiac Care Unit with a swan ganz catheter in place for continuous invasive hemodynamic monitoring

Exclusion Criteria

1. Patient's with fragile skin or skin conditions that would prevent them from having a sensor placed
2. Patients undergoing exercise or drug induced cardiac stress test
3. Patients with a visible wound at site of sensor placement 3.4. Patients with structural or functional limitations to peripheral blood flow (known upper extremity peripheral arterial disease, use of vasopressors etc.).

Trial design

42 participants in 1 patient group

Adults

Description:

Adults scheduled to receive a TTE (Trans-esophogeal echocardiogram)

Treatment:

Device: wearable vital signs sensor