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OpenTrials
Completed

NCT Number: NCT01537133

Airway Microbiome in Asthma: Relationships to Asthma Phenotype and Inhaled Corticosteroid Treatment

There are new, very sensitive methods for detecting bacteria. These methods show that hundreds of millions of microbes (organisms that can only be seen with microscopes), especially bacteria, live in healthy people. The collection of different microbes found in a site is called a "microbiome." The investigators know that microbiomes of the skin, sinuses, mouth, gastro-intestinal tract, etc. differ from each other. The make-up of the microbiome - which bacteria are found in a site - may be necessary for good health. For example, the microbiome of the mouth is different in people with inflammation of the gums (periodontitis), and the microbiome of the bowel is different in people with inflammation of the intestinal tract (inflammatory bowel disease).

The purpose of this research study is to find out if the microbiome in the lungs is different in healthy people without asthma compared to people with asthma. This study will also find out if the microbiome of the lungs changes when people with asthma take a daily "controller" medication called an inhaled corticosteroid.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, San Francisco, Adult, San Francisco, California, United States

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About this study

Two broad specific aims of this study are: 1)To evaluate whether the microbiota of the bronchial airways in atopic asthmatics and atopic healthy controls differ in microbial diversity, richness, evenness, or composition of specific bacterial taxa. 2) To determine whether inhaled corticosteroid treatment alters bronchial microbial community composition in asthmatics.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Asthmatic:

  • History of physician-diagnosed asthma.
  • Methacholine PC20 < 8mg/ml and/or FEV1 improvement ≥ 12% in response to 180 mcg albuterol.
  • FEV1 ≥ 70% of predicted after 180 mcg albuterol.
  • Stable asthma for ≥ 3 months prior to enrollment (no urgent care visits, no systemic corticosteroid treatment).
  • Asthma Control Questionnaire 6 Score < 1.5.
  • Able to provide informed consent.
  • Able to perform spirometry as per ATS criteria.
  • Evidence by allergen skin test of sensitivity to an aeroallergen.
  • Willingness, if female and able to conceive, to utilize one medically-acceptable form of contraception.

Healthy Control:

  • Evidence by allergen skin test of sensitivity to an aeroallergen.
  • Able to provide informed consent.
  • Able to perform spirometry as per ATS criteria.

Exclusion criteria

Asthmatic:

  • Presence of lung disease other than asthma.
  • Use of > 10 doses of nasal corticosteroids in the previous 3 months.
  • Presence of significant medical illness or other chronic diseases whose treatment could affect the clinical features measured, responses to the therapies to be given in this study, or risks of participating in the study.
  • History of atrial or ventricular tachyarrhythmia.
  • Changes suggestive of cardiac ischemia on ECG at baseline.
  • History of upper respiratory infection, sinusitis, bronchitis, or antibiotic use in the previous 3 months.
  • History of chronic sinus disease.
  • Smoking > 5 pack-years, or within the past year
  • History of long-term controller medication use for asthma (inhaled or oral corticosteroid, leukotriene pathway antagonist, cromolyn, or theophylline within the preceding 6 months.
  • History of bleeding disorder.
  • Reduced creatinine clearance.
  • Inability, in the opinion of the Study Investigator, to coordinate use of inhaler or otherwise comply with medication regimens.
  • Contraindication to bronchoscopy on history or examination.

Healthy Control:

  • History of chronic respiratory disease including asthma.
  • Presence of significant medical illness or other chronic diseases whose treatment could affect the clinical features measured, responses to the therapies to be given in this study, or risks of participating in the study.
  • History of atrial or ventricular tachyarrhythmia.
  • Changes suggestive of cardiac ischemia on ECG at baseline.
  • History of upper respiratory infection, sinusitis, bronchitis, or antibiotic use in the previous 3 months.
  • Methacholine PC20 < 16 mg/ml or FEV1 improvement ≥ 12% in response to albuterol.
  • History of chronic sinus disease
  • Smoking > 5 pack-years, or within the past year
  • Use of > 10 doses of a nasal corticosteroid preparation in the previous 3 months
  • FEV1 or FVC < 80% predicted.
  • History of bleeding disorder.
  • Reduced creatinine clearance.
  • Contraindication to bronchoscopy on history or examination.

Treatment and study plan

Fluticasone

Drug

Dry Powder Inhaler: 250 mcg/puff, one puff, twice a day

Other names: Flovent 250

Placebo

Drug

Dry Powder Inhaler: Placebo

Primary outcomes

  1. Microbial Community Richness

    Time frame: baseline and after 6 weeks of treatment

    Richness is the total number of different bacterial taxa detected in the sample.

  2. Microbial Community Diversity

    Time frame: baseline and after 6 weeks of treatment

    The Shannon diversity index is a type of entropy measure and is a function of the distribution of the total number of organisms across all of the species. If S is the total number of species in the sample and p_i is the number of organisms in the i-th species divided by the total number of organisms, then Diversity = -Σ p_i log(p_i).

  3. Microbial Community Evenness

    Time frame: baseline and after 6 weeks of treatment

    Pielou's evenness index is a scaled measure of biodiversity and is equal to the observed Shannon diversity index divided by the maximum possible Shannon diversity index, which would occur if all of the species in the sample were equally abundant. Evenness = D/log(S), where D is the Shannon Diversity index and log(S) is the maximum diversity of the sample.

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Feb 23, 2012
Registry last updated
Nov 30, 2016

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.

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