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Inflammatory Processes in the Airway of Asthmatics With Persistent Bronchial Hyperreactivity

Primary Purpose

Asthma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bronchoscopic
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Asthma focused on measuring asthma, corticosteroids

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Symptoms of asthma as defined by the American Thoracic Society (ATS) definition. This includes the following: history of episodic shortness of breath (with or without associated wheezing) in association with reversible obstructive airways disease with at least a 20% decrement in FEV1 and FVC (from predicted values) that is documented at some time point by pulmonary function tests an improvement in expiratory flow rates of at least 15% of predicted values after inhalation of a beta-2 selective bronchodilator medication or other previous treatment (e.g. corticosteroids) The diagnosis may also be confirmed by an abnormal bronchospastic response to methacholine or exercise as described by Cherniak FEV1 greater than or equal to 70% of predicted value at time of study entry Regular use of inhaled corticosteroids at time of study entry (at least 400 mcg of Beclomethasone or equivalent) Exclusion Criteria: Used inhaled cromolyn (Intal) or nedocromil (Tilade) in the month prior to study entry History of severe asthma requiring intubation Any cardiopulmonary or neurologic abnormality with which the risk of performing the procedure would outweigh the potential benefits (other than asthma) Upper respiratory tract infection or clinical evidence of a sinus infection during the month preceding the test History of cigarette smoking within the 5 years prior to study entry or greater than 10 pack-years total Pregnant or refuses to undergo urine pregnancy testing if female of child-bearing age (women of childbearing potential will not be challenged [methacholine challenge] unless they have had a menstrual period in the last 10 days or a negative pregnancy test within 2 weeks or are practicing adequate contraception)

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Open label inhaled fluticasone

Arm Description

Patients are treated with open label high dose fluticasone for 30 days then discontinued. Comparisons are pre- and post- treatment single arm.

Outcomes

Primary Outcome Measures

change in CD3 positive T cells in the airway submucosa

Secondary Outcome Measures

inflammatory cell markers in the airway (CD4, CD8, CD68, CD45, EG2/MBP, tryptase, and neutrophil elastase)
RANTES expression in airway
FEV1, peak expiratory flows
methacholine PC20
asthma symptom score

Full Information

First Posted
September 19, 2005
Last Updated
June 23, 2017
Sponsor
Washington University School of Medicine
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00217854
Brief Title
Inflammatory Processes in the Airway of Asthmatics With Persistent Bronchial Hyperreactivity
Official Title
Mechanisms of Airway Inflammation: Natural Exacerbation of Asthma Induced by Glucocorticoid Withdrawal
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
September 2001 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to examine inflammatory processes in the airway of moderate to severe persistent asthmatics who have persistent bronchial hyperreactivity despite chronic administration of inhaled glucocorticoids.
Detailed Description
BACKGROUND: The Inhaled Glucocorticoid Withdrawal Protocol will investigate abnormalities in the asthmatic airway that occur in the setting of a "natural" endogenous exacerbation. It is known that chronic treatment with inhaled glucocorticoids causes a nearly complete disappearance of inflammatory cells from the airway and improvement in bronchial hyperreactivity, yet such patients have persistent bronchial hyperreactivity. Withdrawal of inhaled glucocorticoids causes a worsening of bronchial hyperreactivity. These observations suggest that a chronic derangement in the asthmatic airway might exist, which is unmasked by withdrawal of inhaled glucocorticoids and which reinitiates the inflammatory process. These "persistent" abnormalities in the asthmatic airway may be seen during quiescent stages of chronic asthma even when airway inflammatory changes are not evident. The abnormalities may be seen during the period of treatment with inhaled glucocorticoids or they may appear as one of the first signs after the withdrawal of inhaled glucocorticoids, thereby initiating the recurrence of asthma and promoting inflammation. DESIGN NARRATIVE: The purpose of this study is to examine inflammatory processes in the airway of moderate to severe persistent asthmatics who have persistent bronchial hyperreactivity despite chronic administration of inhaled glucocorticoids. Each participant will undergo bronchoscopic procedures and have assessment of bronchial hyperreactivity at the following two time points: 1) during treatment with inhaled fluticasone; and 2) after acute withdrawal of inhaled fluticasone. The primary outcome of this study is the change in CD3 positive T cells in the airway submucosa. The key secondary outcomes are as follows: 1) other inflammatory cell markers in the airway (e.g., CD4, CD8, CD68, CD45, EG2/MBP, tryptase, and neutrophil elastase); 2) RANTES (regulated on activation, normal T expressed and secreted) expression in airway; 3) FEV1 peak expiratory flows; 4) methacholine PC20; and 5) asthma symptom score.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
asthma, corticosteroids

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open label inhaled fluticasone
Arm Type
Other
Arm Description
Patients are treated with open label high dose fluticasone for 30 days then discontinued. Comparisons are pre- and post- treatment single arm.
Intervention Type
Procedure
Intervention Name(s)
Bronchoscopic
Intervention Description
Bronchoscopic procedure
Primary Outcome Measure Information:
Title
change in CD3 positive T cells in the airway submucosa
Time Frame
Measured at Week 4
Secondary Outcome Measure Information:
Title
inflammatory cell markers in the airway (CD4, CD8, CD68, CD45, EG2/MBP, tryptase, and neutrophil elastase)
Time Frame
Measured at Week 4
Title
RANTES expression in airway
Time Frame
Measured at Week 4
Title
FEV1, peak expiratory flows
Time Frame
Measured at Week 4
Title
methacholine PC20
Time Frame
Measured at Week 4
Title
asthma symptom score
Time Frame
Measured at Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptoms of asthma as defined by the American Thoracic Society (ATS) definition. This includes the following: history of episodic shortness of breath (with or without associated wheezing) in association with reversible obstructive airways disease with at least a 20% decrement in FEV1 and FVC (from predicted values) that is documented at some time point by pulmonary function tests an improvement in expiratory flow rates of at least 15% of predicted values after inhalation of a beta-2 selective bronchodilator medication or other previous treatment (e.g. corticosteroids) The diagnosis may also be confirmed by an abnormal bronchospastic response to methacholine or exercise as described by Cherniak FEV1 greater than or equal to 70% of predicted value at time of study entry Regular use of inhaled corticosteroids at time of study entry (at least 400 mcg of Beclomethasone or equivalent) Exclusion Criteria: Used inhaled cromolyn (Intal) or nedocromil (Tilade) in the month prior to study entry History of severe asthma requiring intubation Any cardiopulmonary or neurologic abnormality with which the risk of performing the procedure would outweigh the potential benefits (other than asthma) Upper respiratory tract infection or clinical evidence of a sinus infection during the month preceding the test History of cigarette smoking within the 5 years prior to study entry or greater than 10 pack-years total Pregnant or refuses to undergo urine pregnancy testing if female of child-bearing age (women of childbearing potential will not be challenged [methacholine challenge] unless they have had a menstrual period in the last 10 days or a negative pregnancy test within 2 weeks or are practicing adequate contraception)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario Castro
Organizational Affiliation
Washington University School of Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
14726420
Citation
Castro M, Bloch SR, Jenkerson MV, DeMartino S, Hamilos DL, Cochran RB, Zhang XE, Wang H, Bradley JP, Schechtman KB, Holtzman MJ. Asthma exacerbations after glucocorticoid withdrawal reflects T cell recruitment to the airway. Am J Respir Crit Care Med. 2004 Apr 1;169(7):842-9. doi: 10.1164/rccm.200208-960OC. Epub 2004 Jan 15.
Results Reference
background
Links:
URL
http://pulmonary.wustl.edu/
Description
Click here for the Pulmonary and Critical Care Medicine Website

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Inflammatory Processes in the Airway of Asthmatics With Persistent Bronchial Hyperreactivity

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