Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Children's Hospital Medical Center, Cincinnati
With
Masimo Corporation
Children's Medical Center Dallas
University of Texas Southwestern Medical Center
The study seeks to determine the reliability and accuracy of the acoustic respiratory monitoring (RAM) in comparison of clinically completed transthoracic impedance monitoring (TI) and manual counting of respiratory rate in postoperative pediatric patients at risk of adverse respiratory events.
Age
2–16
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female children 2 to 16 years of age
In-patients or 23 hour short stay patients who had a tonsillectomy with a diagnosis or symptoms of obstructive sleep apnea or who had any surgery and receiving an opioid by patient controlled analgesia for post-operative pain control
Child weighs at least 10 kg on day of surgery
You may not be if
Patient has skin abnormalities (rash, eczema, etc.) at the planned application sites that would interfere with sensor or electrode applications.
Patient is admitted to the Intensive Care Unit
Patient has tracheostomy
Patient is on non-invasive ventilator support
Clareo Health | Evaluation of Respiratory Acoustic Monitor in Children After Surgery