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Clinical Trial Summary

This project will investigate whether reduction in ambient light and elimination of noise during induction and emergence from anesthesia influences the response time of the anesthesia provider to auditory and visual alarms when compared to a standard operating room. In addition, the investigators will assess the cumulative level of noise exposure that providers experience during the perioperative period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03507855
Study type Interventional
Source Nationwide Children's Hospital
Contact
Status Completed
Phase N/A
Start date October 18, 2018
Completion date November 30, 2021

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