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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00250341
Other study ID # IXR-403-4-196
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date September 30, 2005
Est. completion date September 30, 2007

Study information

Verified date November 2021
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a Phase 4, single center study conducted in mild-to moderate asthmatics.


Description:

The study consists of 3 phases. There are 7 study visits.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date September 30, 2007
Est. primary completion date September 30, 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18-65 years old - Currently using SABA prn or a low-to-moderate persistent asthma Exclusion Criteria: - Tobacco use within 1 year or >= 5 pack years

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
QVAR
480 mcg
Advair
250/50 mcg
Servent Diskus
50 mcg

Locations

Country Name City State
United States UCLA Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
Teva Branded Pharmaceutical Products R&D, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary High resolution Cat Scans
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