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Frequency of Ventilator Associated Pneumonia (VAP) in Mechanically Ventilated Patients Using the AnapnoGuard System

Frequency of Ventilator Associated Pneumonia (VAP) in Mechanically Ventilated ICU Patients Using the AnapnoGuard System

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01126320
Enrollment
161
Registered
2010-05-19
Start date
2010-12-31
Completion date
2015-12-31
Last updated
2016-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator Associated Pneumonia

Keywords

VAP

Brief summary

Ventilator Associated Pneumonia (VAP) is a common complication experienced by mechanically ventilated patients and within the framework of Respiratory Intensive Care Units. The AnapnoGuard system, developed by Hospitech Respiration Ltd. is a ventilation guard system that includes a number of unique characteristics. This study was designed to test the frequency VAP in mechanically ventilated ICU patients using the AnapnoGuard System.

Interventions

DEVICEAnapnoGuard 100,

Respiratory guard system during mechanical ventilation with routine mechanical ventilator

DEVICEroutine mechanical ventilator

routine mechanical ventilation

Sponsors

Hospitech Respiration
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ICU patients; * Patient was connected to AnapnoGuard system up to six hours from intubation; * Age - above 18.

Exclusion criteria

* Pneumonia; * Aspiration Pneumonia; * Chronic or Severe Pneumonia; * Chronic Obstructive Pulmonary Disease (COPD) requiring permanent home-based antibiotic treatment; * Interstitial Lung Disease (ILD); * Post Lung Transplant State; * Immunosuppression. * Patients ventilated in prone position * Patient who was ventilated 3 months prior to being enrolled in the study * Pregnant women

Design outcomes

Primary

MeasureTime frame
VAP occurence2 years

Secondary

MeasureTime frame
Adverse events occurence2 years

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026