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Clinical Trial Summary

This is a prospective, single-arm, non-randomized, non-controlled single-center study for the evaluation of the Zynex CM-1600 in 20 healthy adults undergoing a manual blood loss of up to 500mL followed by an infusion of 1 liter of normal saline.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05740644
Study type Interventional
Source Zynex Monitoring Solutions
Contact
Status Completed
Phase N/A
Start date February 13, 2023
Completion date February 22, 2023

See also
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