Recruiting

Wireless Devices

Sponsor:

Ann & Robert H Lurie Children's Hospital of Chicago

Code:

NCT04723654

Conditions

Prematurity

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Accepted

Interventions

Wireless Wearable Vital Sign Monitor

Study Details

Brief summary:

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 ID

NCT04723654

Start date

Mar 15, 2018

Status verified date

Jun, 2026

Completion date

Nov 30, 2028

Anticipated

Primary completion date

Jun 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Accepted

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

Study Design

Enrollment

500 participants

Anticipated

Interventions and Outcome Measures

Arms

ICU Population

Patients admitted to one of 3 ICUs at Lurie Childrens

Non-ICU Population

Healthy volunteers who are under 18 years of age, whose parents consent to their participation, and who are willing to visit CAMP for a one time study visit can participate in this study.

Interventions

Wireless Wearable Vital Sign Monitor

Placement of wireless wearable vital sign monitors on patients limbs for up to 48 hours

Primary outcome measure

  • Continuous non-invasive BP monitoring [ Time Frame: up to 48 hours ]

Central Contacts and Locations

Central contacts

Susan Slattery, MD

312-227-3300sslattery@luriechildrens.org

Casey Rand, MDS

312-227-3300crand@luriechildrens.org

Locations

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

Recruiting

Chicago, Illinois, United States, 60611

Contacts

Susan Slattery, MD

312-227-3300sslattery@luriechildrens.org

Northwestern Medicine Prentice Women's Hospital

Recruiting

Chicago, Illinois, United States, 60611

Contacts

Susan Slattery, MD

312-227-3300sslattery@luriechildrens.org

More Information

Sponsor

Ann & Robert H Lurie Children's Hospital of Chicago

Last update posted

Aug 17, 2026

Last verified

Jun, 2026

Keywords

  • Blood Pressure
  • Vital Signs
  • Wireless Monitoring

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Ann & Robert H Lurie Children's Hospital of Chicago on 2026-08-17.