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OpenTrials
Completed

NCT Number: NCT04142073

CCU Wireless Vital Signs Monitoring

This is a pilot study is to test a wireless, skin-sensor device against current technology in the CCU to monitor vitals

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Key information

Conditions

CCU Inpatients

Age range

0 month–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Northwestern University

Chicago, Illinois, 60611, United States

About this study

This is a single center, prospective, observational study that will recruit subjects from Lurie Children's Hospital to test a wireless vitals monitor against the current vitals monitors used in the Cardiac Care Unit.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients under the age of eighteen admitted to the Lurie's Children's Cardiac Care Unit will be eligible to participate

Exclusion criteria

  • Patients at imminent risk of death
  • Patients with a skin abnormality that precludes assessment
  • Patients with hyperbilirubinemia and requiring a need for UV light

Treatment and study plan

Primary outcomes

  1. Percent agreement with pilot sensor and current standard of vital signs monitoring

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

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

Registry information

Official study title

Advanced Wireless and Wearable Sensors for Patients With Critical Neonatal and Pediatric Congenital Heart Defects

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Oct 29, 2019
Registry last updated
Jul 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.