Trials / Completed
CompletedNCT03496220
Effect of Angulus on Patient-elevation Compliance
Measuring the Effect of Angulus on Patient-elevation Compliance
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Angulus, LLC · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
Ventilator-associated events (VAE) are a scourge of critical care settings and hospital systems at large. There is extensive evidence that ventilator-associated pneumonia (VAP) and related VAEs increase mortality rates in critically ill patients by up to 50%, while simultaneously increasing cost of care. C Best-practice guidelines state that positioning ventilated patients at an angle between 30-45 degrees significantly reduces the potential for VAP and other VAE to develop. While the intent of the guidelines is to govern patient elevation angle, the lack of a mechanism to accurately measure patient elevation requires that nurses rely on the head-of-bed (HOB) protractor - a tool which reflects the angle of the bed, not the patient - to measure compliance. Depending upon the position and posture of the patient in the bed, a patient's elevation angle may be significantly different from the HOB angle. Critical care teams currently rely on built-in HOB protractors and digital inclinometers that measure the angle of the bed not the patient. Angulus, LLC has developed a dual-component Angulus sensor to fill this gap in critical care technology. Angulus enables critical care practitioners to instantaneously understand a patient's elevation, identify when the patient is outside of the desired 30-45 degree recumbency scope, and efficiently correct the patient's orientation with immediate feedback. Angulus supports real-time minute-to-minute data display as well as longitudinal aggregation of data.
Conditions
- Ventilator Adverse Event
- Ventilator Associated Pneumonia
- Hospital Acquired Condition
- Hospital-acquired Pneumonia
- Recumbency
- Head-of-bed
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Angulus | Feedback on patient recumbency |
Timeline
- Start date
- 2018-07-10
- Primary completion
- 2018-09-30
- Completion
- 2018-09-30
- First posted
- 2018-04-12
- Last updated
- 2024-03-06
- Results posted
- 2021-01-19
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03496220. Inclusion in this directory is not an endorsement.