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Clinical Trial Summary

The study is a prospective, non-randomized, non-blinded, non-significant risk, multi-center study enrolling up to 500 healthy adult subjects consented to undergo a whole blood donation procedure. The study will involve enrolling subjects that will undergo blood donation wearing the study device (CM-1600 Device) and capture study-required physiological parameters pre-, during, and post-donation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05463198
Study type Interventional
Source Zynex Monitoring Solutions
Contact
Status Completed
Phase N/A
Start date September 14, 2022
Completion date May 26, 2023

See also
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