World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 16 December 2017
Main ID:  NCT02450279
Date of registration: 18/05/2015
Prospective Registration: Yes
Primary sponsor: Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Public title: Scintigraphic Comparison of Lung Deposition With Two Nebulizers During Invasive Mechanical Ventilation
Scientific title:
Date of first enrolment: March 2016
Target sample size: 20
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/show/NCT02450279
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator).  
Phase:  N/A
Countries of recruitment
Belgium
Contacts
Name:     Pierre-François Laterre
Address: 
Telephone:
Email:
Affiliation:  Head of Intensive Care Unit, Cliniques Universitaires Saint-Luc
Key inclusion & exclusion criteria

Inclusion Criteria:

- Invasive mechanical ventilation

- Healthy lungs

Exclusion Criteria:

- Discontinued procedure due to adverse events.



Age minimum: 18 Years
Age maximum: 90 Years
Gender: All
Health Condition(s) or Problem(s) studied
Post-operative Neurosurgery
Intervention(s)
Device: Vibrating-mesh nebulizer
Drug: technetium-99m - Diethylenetriaminepentaacetic acid
Other: Preoperative spirometry
Device: Jet Nebulizer
Other: Planar scintigraphy
Primary Outcome(s)
Pulmonary deposition [Time Frame: Immediately after nebulization by imaging assessment, an expected average of 30 minutes]
Secondary Outcome(s)
Lung function [Time Frame: Preoperative assessment, the day before inclusion]
Mechanical ventilation settings [Time Frame: During nebulisation time, an expected average of 15 minutes]
Penetration index [Time Frame: Immediately after nebulization by imaging assessment, an expected average of 30 minutes]
Secondary ID(s)
AeroVent-02
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history