Clinical Evaluation of the Zynex Monitoring System, Model CM-1600

Status Completed

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

Fluid Loss

Clinical Trial Details

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

View Details

See also
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