Trials / Completed
CompletedNCT05740644
Clinical Evaluation of the Zynex Monitoring System, Model CM-1600
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Zynex Monitoring Solutions · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CM-1600 | Healthy subjects undergoing a manual blood loss of up to 500mL followed by an infusion of 1 liter of normal saline will be connected to the CM-1600 device. |
Timeline
- Start date
- 2023-02-13
- Primary completion
- 2023-02-22
- Completion
- 2023-02-22
- First posted
- 2023-02-23
- Last updated
- 2024-07-16
- Results posted
- 2024-07-16
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05740644. Inclusion in this directory is not an endorsement.