A Smart, "Always -On" Health Monitoring System
Status: | Recruiting |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | Any |
Updated: | 1/3/2019 |
Start Date: | March 2016 |
End Date: | March 2020 |
Contact: | Dermatology CTU |
Email: | NUdermatologyCTU@northwestern.edu |
Phone: | 312-503-5944 |
A Smart, "Always -On" Health Monitoring System, Sub-Study: No Strings Attached: Wireless Sensor Technology in the Prentice NICU
This is a pilot study is to test a wireless, skin-sensor device against current technology in
the NICU to monitor vitals
the NICU to monitor vitals
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.
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.
Inclusion Criteria:
- 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)
Exclusion Criteria:
- 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
We found this trial at
1
site
Chicago, Illinois 60611
Principal Investigator: Amy Paller, MD
Phone: 312-503-5944
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