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

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

Who can join

Up to age 18 · All sexes · Healthy volunteers welcome

Inclusion Criteria-ICU Population:

* Admitted to one of the four ICUs at Lurie Children's or Prentice Women's Hospital
* Under 18 years of age

Inclusion Criteria-Non-ICU Population

* Under 18 years of age
* Willing to visit the Center for Autonomic Medicine in Pediatrics (CAMP) for a one time study visit

Exclusion Criteria-ICU Population:

* A skin abnormality that would potentially increase the risk of device
* 18 years of age or older
* Determined by an attending physician or bedside care team to be too unstable (patient) or experiencing too much stress (family)

Exclusion Criteria-Non-ICU Population:

* A skin abnormality that would potentially increase risk of device use
* 18 years of age or older

About the study

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.

What is being tested

• Wireless Wearable Vital Sign Monitor (device)

Sponsor: Ann & Robert H Lurie Children's Hospital of Chicago · Participants: 500 · Started: Mar 15, 2018

Contact the study team

• Susan Slattery, MD · Phone: 312-227-3300
• Casey Rand, MDS · Phone: 312-227-3300

Official record on ClinicalTrials.gov — NCT04723654

Locations in the U.S.

Conditions

• Premature Birth

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.