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Clinical Trial Summary

Time to stable reading of oxygen saturation at the delivery room will be compared between two different devices.


Clinical Trial Description

After delivery babies will be located in the radiant warmer. The probe of each pulse oximeter will be applied to one of the feet. Both probes will be simultaneously connected to the female plug of the pulse oximeter.

Heart rate will be checked

Time to get a stable reading in each device (by observation on the devices' display) will be recorded; this will be the primary study outcome. Other vital signs (oxygen saturation, heart rate) and demographics) will be recorded as well.

Paired students T test will be used for the statistical analyzes. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02704585
Study type Interventional
Source Shaare Zedek Medical Center
Contact Yakir Shir, MD
Phone 972523121040
Email yakirshir@gmail.com
Status Recruiting
Phase N/A
Start date January 2016
Completion date January 2017

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