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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00559689
Other study ID # Hamamatsu-17-43
Secondary ID H-17-43
Status Completed
Phase Phase 4
First received November 15, 2007
Last updated March 13, 2009
Start date November 2005
Est. completion date March 2007

Study information

Verified date March 2009
Source Hamamatsu University
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational

Clinical Trial Summary

Once-daily inhaled glucocorticosteroids treatment can sufficiently control airway inflammation in asthma patients.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date March 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Receive ICS for one year or more, with no change in dose within the previous 8 weeks

Exclusion Criteria:

- Two or more courses of oral corticosteroid in the previous 12 months

- Admission to hospital due to asthma in the previous 6 months

- Admission to the intensive care unit due to asthma at any time in the past

- Current cigarette smoker.

Study Design

Observational Model: Case-Crossover, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Drug:
Budesonide,hydrofluoroalkane-beclomethasone dipropionate
receive twice-daily administration
Budesonide,hydrofluoroalkane-beclomethasone
once-daily administration at bedtime

Locations

Country Name City State
Japan Hamamatsu University School of Medicine Hamamatsu

Sponsors (1)

Lead Sponsor Collaborator
Hamamatsu University

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary once-daily administration of inhaled glucocorticosteroids can control airway inflammation two-year
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