Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Northwestern University
This is a single center, prospective, observational study that will recruit subjects from Lurie Children's Hospital and Prentice Women's Hospital to test a new wireless vitals monitor against the current vitals monitors used in the NICU. Patients will be neonates in different age brackets.
Age
0–0
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Neonates in different age cohorts from ages 25 weeks gestational age to fullterm infants or infants up to 6 months of age, selected with assistance of NICU staff
Currently in NICU and requiring monitoring for heart rate, ECG, respiratory rate, temperature, and pulse oximetry
Parents able to understand and provide informed consent for study
Infants enrolled in the Pre-Vent study (sub-study only)
You may not be if
Over 6 months of age
Hemodynamic or other instability precluding testing of new monitoring with concurrent standards
Infants at imminent risk of death and neonates with a skin abnormality that precludes assessment
