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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00980707
Other study ID # AI-005 versican
Secondary ID
Status Completed
Phase Phase 4
First received September 17, 2009
Last updated January 18, 2012
Start date August 2009
Est. completion date November 2010

Study information

Verified date January 2012
Source Associated Scientists to Help Minimize Allergies
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the role of versican and hyaluronan measurements in induced sputum as biomarkers of asthma. Enroll 10 subjects with mild persistent asthma who are not receiving treatment with a controller therapy.


Description:

We will compare spirometry, eNO and sputum measurements of versican and hyaluronan before and after treatment with fluticasone 220 ug/bid.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date November 2010
Est. primary completion date June 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Allergic asthma defined as a positive methacholine challenge

Exclusion Criteria:

- Non-atopic patients

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Drug:
Inhaled corticosteroid (fluticasone)
inhaled fluticasone 220 ug/bid

Locations

Country Name City State
United States Associated Scientists to Help Minimize Allergies Seattle Washington

Sponsors (3)

Lead Sponsor Collaborator
Associated Scientists to Help Minimize Allergies Benaroya Research Institute, GlaxoSmithKline

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compare hyaluronan and versican in asthmatics versus atopic non-asthmatics. 1 year No
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