Evaluating Wearable Smart Sensors for Continuous Measurement of Vital Signs in ICU Patients

Description

The purpose of this study is to develop biocompatible wireless electronic devices that will allow continuous, non-invasive hemodynamic and physiology measurements in the ICU.

Conditions

Prematurity

Study Overview

Study Details

Study overview

The purpose of this study is to develop biocompatible wireless electronic devices that will allow continuous, non-invasive hemodynamic and physiology measurements in the ICU.

Evaluating Wearable Smart Sensors for Continuous Measurement of Vital Signs in ICU

Evaluating Wearable Smart Sensors for Continuous Measurement of Vital Signs in ICU Patients

Condition
Prematurity
Intervention / Treatment

-

Contacts and Locations

Chicago

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United States, 60611

Chicago

Northwestern Medicine Prentice Women's Hospital, Chicago, Illinois, United States, 60611

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    to 18 Years

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    Yes

    Collaborators and Investigators

    Ann & Robert H Lurie Children's Hospital of Chicago,

    Study Record Dates

    2026-06-30