Trials / Completed
CompletedNCT05673174
Avicena LVDP Validation Study in Healthy Volunteers
Assessment of the Vivio System for the Non-Invasive Estimation of Left Ventricular Diastolic Pressure (LVDP) in Healthy Volunteers
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 321 (actual)
- Sponsor
- Avicena LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to document the utility of the Vivio System in quantifying LVDP in healthy volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Non-Invasive Estimation of Left Ventricular Diastolic Pressure | Modified blood pressure cuff used to detect arterial waveforms used for the estimation of LVDP |
Timeline
- Start date
- 2022-06-16
- Primary completion
- 2022-08-30
- Completion
- 2022-08-30
- First posted
- 2023-01-06
- Last updated
- 2023-01-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05673174. Inclusion in this directory is not an endorsement.