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Role of Cigarette Smoking in Regulating Allergen-induced Early and Late Responses in Mild Asthmatics

Primary Purpose

Asthma

Status
Completed
Phase
Early Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Allergen Challenge
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Asthma focused on measuring smoking, asthma, sputum

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects with mild atopic asthma, presently well controlled on ß2-agonist only.
  • Baseline FEV1 more than or equal to 70% of predicted normal.

Exclusion Criteria:

  • Past or present cardiovascular, renal, liver or endocrine disease.
  • Airway infection during the last 4 weeks.
  • Exacerbation during the last 4 weeks.
  • Inhaled or oral steroids during the last 4 weeks.
  • Anti-asthma medication other than inhaled and/or oral ß2-agonists during the last 4 weeks.
  • Pregnant or lactating women or women actively seeking pregnancy or lack of adequate contraception.

Sites / Locations

  • McMaster University

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

1

Arm Description

Allergen challenge

Outcomes

Primary Outcome Measures

To measure the number of inflammatory cells in induced sputum following allergen challenge in smoking and non-smoking asthmatic subjects.

Secondary Outcome Measures

Full Information

First Posted
February 20, 2008
Last Updated
April 23, 2013
Sponsor
Hamilton Health Sciences Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00626171
Brief Title
Role of Cigarette Smoking in Regulating Allergen-induced Early and Late Responses in Mild Asthmatics
Official Title
A Study Evaluating the Role of Cigarette Smoking in Regulating Allergen-induced Early and Late Responses in Mild Asthmatics.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
July 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hamilton Health Sciences Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to determine the effect of cigarette smoking on inflammatory cell recruitment to the lungs after an allergen challenge, in non-smoking and currently smoking mild asthmatic subjects. When comparing non-smoking asthmatics to smoking asthmatics, do differential cell counts obtained from inflammatory cells in induced sputum after allergen challenge differ? Will differential cell counts show a decline in inflammatory cells in the induced sputum of asthmatics who have refrained from smoking for eight weeks? This study is a randomized, case-controlled study. The first part of the study requires smoking and non-smoking subjects who will attend 2 study periods of 3 consecutive days (triad). In each triad, they will be challenged with allergen or diluent by inhalation, in a random order, and each triad is separated by a washout period. In the second part of the study, current smokers will be invited to undergo another allergen challenge 8 weeks of smoking cessation.
Detailed Description
10 non-smoking adult subjects and 10 smoking adult subjects with mild atopic asthma will be studied. Part 1: On the first study day of the triad, subjects will undergo screening procedures, including complete history and physical examination. Methacholine inhalation challenge and allergen skin titration will be performed to determine the concentration of allergen required for inhalation. Sputum will be induced for baseline measurement of airway inflammatory cells. On the second day, subjects will inhale the allergen or diluent in randomized order, and spirometry will be measured for the next 7 hours. Sputum will be collected at 7 hours after challenge. On the third day, subjects will report to the lab 24 hours after allergen/diluent inhalation challenge. Sputum cells will be collected to measure the percentage of airway inflammatory cells, including eosinophils and neutrophils. After washout of 2-4 weeks, subjects will return to undergo diluent/allergen triad. Part 2: Asthmatic smokers will be studied to investigate allergen-induced changes in inflammatory cell numbers after they quit smoking for a period of 8 weeks. Asthmatic smokers who were involved in the first part of the study will be asked if they would like to participate in this part of the study, and they will be provided with smoking cessation tools including nicorette gum and nicotine patches, to aid them in ceasing to smoke. At the beginning of the study period, the same procedures that occurred in part 1 will be performed to obtain initial baseline results- ie- history, physical examination, skin prick test, methacholine challenge and sputum induction. Throughout the 8 week period, subjects will be required to come in weekly to perform a carboxyhemoglobin test, to ensure that they have not been smoking that week. At the end of the 8 week period, an allergen challenge triad will be carried out (as was performed in Part 1 of the study). Those subjects who were not able to comply to the smoking cessation regime will still be included in the final measurements. We hypothesize that inflammatory cell counts will be higher in the asthmatic smokers versus asthmatic non-smokers. We also hypothesize that subjects who quit smoking for the 8 week period will show a decline in inflammatory cell counts indicating an improvement in lung function. We believe that the results of this novel study will provide greater insight into the inflammatory response in asthmatic smokers, and will suggest appropriate therapeutic approaches for control of asthma in smokers.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Other
Arm Description
Allergen challenge
Intervention Type
Procedure
Intervention Name(s)
Allergen Challenge
Intervention Description
Allergen challenge
Primary Outcome Measure Information:
Title
To measure the number of inflammatory cells in induced sputum following allergen challenge in smoking and non-smoking asthmatic subjects.
Time Frame
7h and 24 h post

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects with mild atopic asthma, presently well controlled on ß2-agonist only. Baseline FEV1 more than or equal to 70% of predicted normal. Exclusion Criteria: Past or present cardiovascular, renal, liver or endocrine disease. Airway infection during the last 4 weeks. Exacerbation during the last 4 weeks. Inhaled or oral steroids during the last 4 weeks. Anti-asthma medication other than inhaled and/or oral ß2-agonists during the last 4 weeks. Pregnant or lactating women or women actively seeking pregnancy or lack of adequate contraception.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul O'Byrne, MD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gail Gauvreau, PhD
Organizational Affiliation
McMaster University
Official's Role
Study Director
Facility Information:
Facility Name
McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 3Z5
Country
Canada

12. IPD Sharing Statement

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Role of Cigarette Smoking in Regulating Allergen-induced Early and Late Responses in Mild Asthmatics

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