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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01877304
Other study ID # AKITA
Secondary ID
Status Completed
Phase N/A
First received May 29, 2013
Last updated June 10, 2013
Start date June 2010
Est. completion date March 2013

Study information

Verified date June 2013
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Interventional

Clinical Trial Summary

To compare deposition between two modalities of nebulization


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Free of respiratory disease

Exclusion Criteria:

- Smokers

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
AKITA


Locations

Country Name City State
Belgium Cliniques universitaires Saint-Luc Brussels

Sponsors (1)

Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lung deposition by scintigraphy After 15 minutes No
Secondary Regional deposition by scintigraphy After 15 minutes No
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