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

Recruiting Observational Study
Prematurity
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
Up to 18
Sex
Any
Study type
Observational
Participants needed
500 (estimated)
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
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 stu…
Contacts

Susan Slattery, MD

312-227-3300

sslattery@luriechildrens.org

CONTACT

Casey Rand, MDS

312-227-3300

crand@luriechildrens.org

CONTACT