Trials / Completed
CompletedNCT04215627
Comparing the PiCCO Monitor to the Non-invasive Biobeat (BB)-316PW in ICU Patients
Comparison Between Invasive Hemodynamic Monitoring, Using the PiCCO Monitor, to a Non-invasive Photoplethysmography Based Device in Hemodynamic Unstable Critically Ill Patients, With Vasopressor Support
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 9 (actual)
- Sponsor
- Biobeat Technologies Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 99 Years
- Healthy volunteers
- —
Summary
The aim of this study is to compare hemodynamic monitoring using the invasive PiCCO device to the BB-613PW wireless, non-invasive PPG-based device, in critically ill patients within the ICU, suffering from hemodynamic instability and in need of vasopressor support. Data will be gathered prospectively and analysed retrospectively.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | non-invasive monitoring | Comparing the PiCCO monitor to the non-invasive BB-613PW device in hemodynamically unstable critically ill patients in the ICU |
Timeline
- Start date
- 2019-12-26
- Primary completion
- 2021-04-15
- Completion
- 2021-04-30
- First posted
- 2020-01-02
- Last updated
- 2021-07-07
Locations
1 site across 1 country: Israel
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04215627. Inclusion in this directory is not an endorsement.