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NCT01846195 Clinical Trial

Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Patients During a Blood Draw

Blood Loss Clinical Trial

Official title:
Clinical Evaluation of the Zynex Blood Volume Monitor (CM-1500) in Healthy Adult Patients During a Blood Draw

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01846195
Other study ID # Zynex500
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 6, 2012
Est. completion date March 20, 2013

Study information
Verified date October 2022
Source Zynex Monitoring Solutions
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Non-invasive monitoring to measure changes in blood volume.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date March 20, 2013
Est. primary completion date March 20, 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Healthy volunteers - Between 18-35 years of age - Weight between 130-200 pounds Exclusion Criteria: - Known cardiac disease - Recent caffeine intake - Tobacco use in the (4) hours prior to screening - Infection - Pregnancy - Hemoglobin <13.5 g/dl

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• CM 1500

Locations
Country Name City State
United States Premier Research Group Salt Lake City Utah

Sponsors (2)
Lead Sponsor Collaborator
Zynex Monitoring Solutions DTarget

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Detect by Non-invasive Monitoring a Change in Blood Volume During a Whole Blood Draw Detection by non-invasive monitoring a change in blood volume (yes or no) during a whole blood draw At study completion (completion of blood draw)
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