Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Volunteers During a Blood Draw
Completed · Phase 1
Conditions studied: Blood Loss
In brief
To determine if a manual blood loss can be detected using the non-invasive blood monitor.
Key facts
- Study ID
- NCT01834612
- Run by
- Zynex Monitoring Solutions
- People needed
- 20
- Starts
- 2013-01-07
- Expected to finish
- 2013-03-11
- Last updated by the study team
- 2021-07-21
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- healthy volunteer
- between 18 to 50 years of age
- weight between 157 to 220 lbs
You may not qualify if…
- 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
Where it is running
- DaVita Clinical Research — Lakewood, Colorado, United States
Full record on ClinicalTrials.gov
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