RECRUITING

Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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. The investigators are interested in determining whether the large and/or small airways are the predominant site of airflow limitation. The investigators are also interested in determining whether intrinsic small airways obstruction and/or loss of lung elastic recoil is responsible for expiratory airflow limitation. The investigators 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.

Official Title

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

Quick Facts

Study Start:2007-10
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01225913

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:10 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Current non-smoking (\<10 pack yr smoking history)
  2. * Stable, treated asthmatics
  3. * Age 10-80 yr
  4. * post 180ug albuterol by MDI: FEV 1/FVC \< 70% and FEV 1 \<80% predicted
  1. * Pregnancy

Contacts and Locations

Study Contact

Arthur F Gelb, MD
CONTACT
562-633-2204
afgelb@msn.com

Principal Investigator

Arthur F Gelb, MD
PRINCIPAL_INVESTIGATOR
Arthur F Gelb Medical Corporation

Study Locations (Sites)

Arthur F Gelb Medical Corporation
Lakewood, California, 90712
United States

Collaborators and Investigators

Sponsor: Gelb, Arthur F., M.D.

  • Arthur F Gelb, MD, PRINCIPAL_INVESTIGATOR, Arthur F Gelb Medical Corporation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2007-10
Study Completion Date2027-06

Study Record Updates

Study Start Date2007-10
Study Completion Date2027-06

Terms related to this study

Keywords Provided by Researchers

  • asthma
  • lung function
  • inflammation

Additional Relevant MeSH Terms

  • Asthma