Non-invasive Measures of Distal Lung Disease in Asthmatics
- Registration Number
- NCT00250341
- Lead Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Brief Summary
This is a Phase 4, single center study conducted in mild-to moderate asthmatics.
- Detailed Description
The study consists of 3 phases. There are 7 study visits.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
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
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description QVAR Servent Diskus - Advair Advair - QVAR QVAR -
- Primary Outcome Measures
Name Time Method High resolution Cat Scans
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the effects of Servent Diskus, Advair, and QVAR on distal lung disease in asthma?
How does the efficacy of distal lung-targeted therapy compare to standard-of-care in mild-to-moderate asthma patients?
Which biomarkers correlate with treatment response to inhaled corticosteroids in NCT00250341 asthma study?
What are the long-term safety profiles of Servent Diskus, Advair, and QVAR in Phase 4 asthma trials?
Are there combination therapies involving Servent Diskus or Advair that improve distal lung function in asthma?
Trial Locations
- Locations (1)
UCLA
🇺🇸Los Angeles, California, United States
UCLA🇺🇸Los Angeles, California, United States