What this study is
The purpose of this study is to evaluate the site and mechanisms responsible for expiratory airflow limitation in chronic, treated, non-smoking, stable asthmatics with moderate to severe persistent expiratory airflow obstruction. Treatment will include inhaled corticosteroids and long acting beta2agonists and long acting muscarinic antagonists. We are interested in determining whether the large and/or small airways are the predominant site of airflow limitation. We are also interested in determining whether intrinsic small airways obstruction and/or loss of lung elastic recoil is responsible for expiratory airflow limitation and to what extent may be attributed to loss of lung elastic recoil vs decreased airway conductance in peripheral airways. We are also interested to evaluate the role of varying doses of inhaled corticosteroids to suppress large and small airway inflammation using exhaled nitric oxide as surrogate markers of inflammation. For comparison purposes, spirometry and measurements of exhaled nitric oxide will also be obtained if possible during a naturally occurring exacerbation of asthma. High resolution thin section CT of the lung will also be obtained. Analysis will evaluate integrity of the lung parenchyma as to absence and or presence of emphysema and extent of emphysema using voxel quantification. We will also investigate optical coherence tomography to detect clinically unsuspected emphysema. We will also obtain autopsy material when available in asthmatics who expire. Will also measure serum periostin as a marker of inflammation by collaborating with Genetech in San Francisco.
What's being tested
- budesonide/formoterol
Intervention · DRUG
2 inhalations 2X/daily in treated arm/group. No placebo group
- fluticasone/salmeterol
Intervention · DRUG
fluticasone 100ug/salmeterol 50ug, 1 inhalation bid noplacebo fluticasone 250ug/salmeterol 50ug, 1 inhalations bid no placebo Spiriva handihaler daily or respihaler 2 inhalations daily no placebo group
- mometasone/formoterol
Intervention · DRUG
200/5 mcg two puffs bid 100/5 mcg two puffs bid Breo Ellipta once daily Spiriva capsule handihaler once daily or Spiriva respihaler 2 in no placebo group
- Prednisone
Intervention · DRUG
0-15 mg daily as needed
Study details
- Official title
- Evaluation of Mechanism(s)Limiting Expiratory Airflow in Chronic, Stable Asthmatics Who Are Non-smokers
- Sponsor
- Gelb, Arthur F., M.D.
- Conditions
- Asthma
- Enrolling
- 60 people
- Starts
- 2007-10-25
- Est. completion
- 2027-06
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 10 Years – 95 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Current non-smoking (<10 pack yr smoking history)
- Stable, treated asthmatics
- Age 12-95 yr
- Post 180ug albuterol by MDI: FEV 1/FVC < 70% and FEV 1 <80% predicted
You can't join if
- Pregnancy
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openArthur F Gelb Medical Corporation
Lakewood, California, United States
- Arthur F Gelb, MD · Principal investigator
Recruiting
Study team
Sponsor
Gelb, Arthur F., M.D.
Study ID 20070934
Principal investigator
Arthur F Gelb, MD
Arthur F Gelb Medical Corporation
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.