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

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Study ID
NCT04723654
Status
Recruiting
Apply to this trial

Conditions

  • Prematurity

Eligibility Criteria

Sex
ALL
Age
N/A - 18 Years
Healthy Volunteers
Accepted

Interventions

  • Wireless Wearable Vital Sign Monitor — DEVICE
    Placement of wireless wearable vital sign monitors on patients limbs for up to 48 hours

Study Details

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.

Key Dates

Start date
Mar 15, 2018
Status verified
Nov 2024
Primary completion
Dec 31, 2025
Completion
Jun 30, 2026

Study Design

Enrollment
500 participants (estimated)

Arms

  • Arm: ICU Population
    Patients admitted to one of 3 ICUs at Lurie Childrens
  • Arm: 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.

Primary Outcome Measure

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

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Ann & Robert H. Lurie Children's Hospital of ChicagoChicagoIllinois60611
Susan Slattery, MD
[email protected]
312-227-3300
Northwestern Medicine Prentice Women's HospitalChicagoIllinois60611
Susan Slattery, MD
[email protected]
312-227-3300

Find similar trials in Chicago, IL

By research site
Ann & Robert H. Lurie Children's Hospital of Chicago· Chicago, ILNorthwestern Medicine Prentice Women's Hospital· Chicago, IL

Related Studies