Status:

COMPLETED

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

Lead Sponsor:

Zynex Monitoring Solutions

Conditions:

Blood Loss

Eligibility:

All Genders

18-50 years

Phase:

PHASE1

Brief Summary

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

Eligibility Criteria

Inclusion

  • healthy volunteer
  • between 18 to 50 years of age
  • weight between 157 to 220 lbs

Exclusion

  • unstable or untreated cardia disease
  • alcohol consumption in 24 hours prior to screening
  • tobacco use in 4 hours prior to screening
  • pregnancy
  • infection
  • Hemoglobin \< 12.5 g/dL at time of procedure

Key Trial Info

Start Date :

January 7 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 11 2013

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT01834612

Start Date

January 7 2013

End Date

March 11 2013

Last Update

July 21 2021

Active Locations (1)

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Page 1 of 1 (1 locations)

1

DaVita Clinical Research

Lakewood, Colorado, United States, 80228

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