Trials / Completed
CompletedNCT02641327
Monitoring Changes in Blood Pressure
Protocol for Evaluation of EarlySense: A Contact-less Device for Monitoring Changes in Blood Pressure
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- EarlySense Ltd. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The study objective is to assess the accuracy of Earlysense contactless monitoring to detect changes in blood pressure vs. Gold reference method / devices including ambulatory blood pressure monitoring device (ABPM) or invasive blood pressure monitoring for patients who have arterial line as part of their standard clinical care.
Detailed description
The study objective is to collect data to assess the accuracy and reliability of Earlysense contactless monitoring for blood pressure monitoring vs. gold reference methods such as ABPM (Ambulatory blood pressure measurement) for patients hospitalized in Internal Medicine department and vs. Arterial Line measurements for patients hospitalized in ICU. In addition the collected data will be used to further enhance and improve the existing algorithms.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | EarlySense (Passive monitoring) | Passive contact-free monitoring |
Timeline
- Start date
- 2015-12-01
- Primary completion
- 2016-11-01
- Completion
- 2016-11-01
- First posted
- 2015-12-29
- Last updated
- 2016-12-01
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02641327. Inclusion in this directory is not an endorsement.