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Clinical Trial Summary

The study is a prospective, non-randomized, non-blinded, non-significant risk study enrolling up to 60 healthy adult subjects consented to undergo a 1-unit whole blood draw procedure. Subjects will wear the study device (CM-1500) while positioned in either a supine or reclined position during the blood draw and study-required physiological parameters will be captured pre-, during, and post-donation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05980013
Study type Interventional
Source Zynex Monitoring Solutions
Contact
Status Completed
Phase N/A
Start date August 28, 2023
Completion date April 10, 2024

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