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Clinical Trials/NCT02084043
NCT02084043
Completed
Not Applicable

In Vitro Comparison of Continuous and Breath-synchronized Vibrating Mesh Nebulizer During Non Invasive Ventilation: Analysis of Inhaled and Lost Doses.

University Hospital St Luc, Brussels1 site in 1 country3 target enrollmentMarch 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Diseases
Sponsor
University Hospital St Luc, Brussels
Enrollment
3
Locations
1
Primary Endpoint
Inhaled dose
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Using an adult lung bench model of non invasive ventilation, the aim of the study is to compare an experimental system of breath-synchronized vibrating mesh nebulizer to a conventional vibrating mesh nebulizer during non invasive ventilation in terms of inhaled and lost doses.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
June 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University Hospital St Luc, Brussels
Responsible Party
Principal Investigator
Principal Investigator

Jean-Bernard Michotte

MSc, PhD Student

University of Applied Sciences of Western Switzerland

Eligibility Criteria

Inclusion Criteria

  • Not applicable (in vitro study)

Exclusion Criteria

  • hypersensitivity (allergic) reactions to aminoglycosides

Outcomes

Primary Outcomes

Inhaled dose

Time Frame: after 24 hours

The inhaled dose assessed by residual gravimetric method

Secondary Outcomes

  • Expiratory wasted dose(after 24 hours)

Study Sites (1)

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