Skip to main content
OpenTrials
Recruiting

NCT Number: NCT00576069

Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

10 year–95 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Arthur F Gelb Medical Corporation

Lakewood, California, 90712, United States

Location status: Recruiting

Location contact

Arthur F Gelb, MD

PRINCIPAL_INVESTIGATOR

About this study

Results will be evaluated during exacerbation and when stable following treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • Pregnancy

Treatment and study plan

budesonide/formoterol

Drug

2 inhalations 2X/daily in treated arm/group. No placebo group

Other names: symbicort 80/4.5, symbicort 160/4.5, budesonide 80 or 160ug/formoterol 4.5ug, 2 inhalations bid, spiriva handihaler or respihaler

fluticasone/salmeterol

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

Other names: advair 100/50, advair 250/50

mometasone/formoterol

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

Other names: Dulera

Prednisone

Drug

0-15 mg daily as needed

Other names: medrol

Primary outcomes

  1. use exhaled nitric oxide as a surrogate marker of large airway vs small airway/lung inflammation following various doses of inhaled corticosteroids

    Time frame: 20-60 days

  2. determine site of airflow limitation, whether predominantly large and /or small airways using expiratory flow volume curves obtained before and after asthmatics breathe a 80% helium-20% oxygen gas mixture

    Time frame: 20-60 days

  3. investigate the mechanisms that limit expiratory airflow: intrinsic airway obstruction vs loss of lung elastic recoil

    Time frame: 20-60 days

  4. determine the extent of asthma and distribution of emphysema

    Time frame: within 10 days following death or explanted lung if lung transplant obtained

    at autopsy or post lung transplantation

Secondary outcomes

  1. dynamic hyperinflation

    Time frame: 20-60 days

  2. Evaluate large and small airways and lung parenchyma in autopsied or transplanted lung in asthmatics and look for unsuspected emphysema

    Time frame: June 2018

    If approved by surviving power of attorney, chronic non-smoking asthmatics who expire will undergo autopsy evaluation to evaluate extent of airway obstruction as well as presence of emphysema

  3. Optical Coherence Tomography

    Time frame: June 2015

    When stable, chronic non-smoking asthmatics with persistent expiratory airflow obstruction will undergo OCT via flexible bronchoscopy to detect unsuspected emphysema.

Study contacts

Contact information is provided by the study sponsor or research team.

Arthur F Gelb, MD

CONTACT

[email protected]

562-633-2204

Sponsors and collaborators

Lead sponsor

Gelb, Arthur F., M.D.

Indiv

Registry information

Official study title

Evaluation of Mechanism(s)Limiting Expiratory Airflow in Chronic, Stable Asthmatics Who Are Non-smokers

Important dates

Study start
2007
Primary completion
2027
Study completion
2027
First posted
Dec 18, 2007
Registry last updated
Oct 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.