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

NCT01834612 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-07-21

No results posted yet for this study

Summary

To determine if a manual blood loss can be detected using the non-invasive blood monitor.

Conditions

  • Blood Loss

Interventions

DEVICE

CM1500

blood volume monitor

Sponsors & Collaborators

  • Zynex Monitoring Solutions

    lead INDUSTRY

Principal Investigators

  • Chris Galloway, MD · Davita Clinical Research

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-01-07
Primary Completion
2013-03-11
Completion
2013-03-11

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01834612 on ClinicalTrials.gov