This observational clinical trial is designed to confirm whether RESP™ Biosensor could be deployed to support clinical decision making in challenging pediatric cases, minimize clinician-to-clinician variability in lung sound interpretation, obviate the need to disrupt change of shift or chart rounds with physicians, and create a durable archive of the patient's lung sounds for longitudinal comparison within or across hospitalizations.
Study Type
OBSERVATIONAL
The RESP Biosensor will be placed on the patient for periodic recording of auscultory sound.
Memorial Health University Medical Center
Savannah, Georgia, United States
Qualification and verification of lung sounds in pediatric population using RESP Biosensor
Time frame: Periodic recording over 24 hours for inpatient stay
Acceptability and utilization of RESP Biosensor in clinicians, healthcare staff and patient families
Time frame: Periodic recording over 24 hours for inpatient stay
Limitations such as age in pediatric patients
Time frame: Periodic recording over 24 hours for inpatient stay
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