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CysLT1-r Expression Following Allergen Exposure in Asthma and Allergic Rhinitis

Primary Purpose

Asthma, Allergic Rhinitis

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Allergen challenge
Allergen challenge
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Asthma

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • To have a positive reaction to one or more allergen on prick tests.
  • Non smokers
  • No respiratory track infection for at least one month prior to the study.
  • Asthmatic subjects using only inhaled beta-2 agonists on an as needed basis for their asthma treatment.
  • Asthmatic subjects with a history of asthma of at least 6 months.
  • Asthmatic subjects with PC20 methacholine lower or equal to 8 mg/ml.
  • Allergic rhinitic subjects never experienced any asthma symptoms or took any asthma medication in the past.
  • Allergic rhinitic subjects with a PC20 methacholine higher than 16 mg/ml.

Exclusion Criteria:

  • Smokers or ex smokers less than 6 months or more than 10 pack-years.
  • Asthmatic subjects using or used in the past 3 months inhaled or oral corticosteroids.

Sites / Locations

  • Centre de recherche de l'Hopital LavalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Conventional allergen challenge: increasing allergen doses given by nebulisation through the mouth and stopped when a 20% fall in forced expiratory volume in one second is obtained. Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.

Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.

Outcomes

Primary Outcome Measures

Change in CysLT1-r following allergen challenge

Secondary Outcome Measures

Change in CysLT1-r following low dose allergen challenge
Difference in CysLT1-r expression in asthma and allergic rhinitis

Full Information

First Posted
February 27, 2008
Last Updated
May 7, 2008
Sponsor
Laval University
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1. Study Identification

Unique Protocol Identification Number
NCT00631254
Brief Title
CysLT1-r Expression Following Allergen Exposure in Asthma and Allergic Rhinitis
Official Title
Modulation of the CysLT1-r Expression Following Allergen Exposure in Non Asthmatic Subjects With Allergic Rhinitis and Mild Allergic Asthmatic Subjects Using the Induced Sputum Technique.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Unknown status
Study Start Date
October 2003 (undefined)
Primary Completion Date
January 2009 (Anticipated)
Study Completion Date
January 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Laval University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Cysteinyl leukotrienes (CysLTs) play an important role in asthma. CysLTs exert most of their bronchoconstrictive and pro-inflammatory effects through activation of the CysLT1-r. As allergic rhinitis appears to be a predisposing factor in the development of asthma and as CysLT-receptors seem to be implicated in the first steps of asthma manifestations, we think it would be of interest to determine if the CysLT1-r is a key mediator in the progression from allergic rhinitis to asthma. We believe it would be interesting to study the expression of the CysLT1-r Our goal is to assess baseline, as well as variations following allergen bronchoprovocations, in the expression of the CysLT1-r in mild asthmatic subjects compared with non asthmatic subjects with allergic rhinitis. Our hypothesis is that there will be a higher baseline expression of the CysLT1-r in asthmatic subjects compared with allergic rhinitis subjects and that allergen bronchoprovocations will induce an increase in the expression of the CysLT1-r in both groups.
Detailed Description
We will recruit mild allergic asthmatic subjects and non asthmatic subjects with allergic rhinitis. On a baseline visit, allergy skin prick tests, spirometry, methacholine bronchoprovocation and induced sputum (IS) with differential leukocyte count will be obtained. In a second step, mild asthmatic subjects will undergo conventional bronchial allergen challenge. IS will be obtained at 6h (corresponding to the late asthmatic response) and 24h following the challenge. The rhinitic subjects and asthmatic subjects will undergo a 4-day low dose allergen bronchial challenge as well as a nasal allergen challenge. Sputum samples will be obtained following days 2 and 4 of the low dose challenge and one week later, and 24h following nasal challenge. Induced sputum will be analyzed for differential cell count. Total mRNA will be extracted from IS cells and used for RT-PCR.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Allergic Rhinitis

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Conventional allergen challenge: increasing allergen doses given by nebulisation through the mouth and stopped when a 20% fall in forced expiratory volume in one second is obtained. Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.
Intervention Type
Procedure
Intervention Name(s)
Allergen challenge
Intervention Description
Conventional allergen challenge: increasing allergen doses given by nebulisation through the mouth and stopped when a 20% fall in forced expiratory volume in one second is obtained. Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.
Intervention Type
Procedure
Intervention Name(s)
Allergen challenge
Intervention Description
Low dose allergen challenge: very low allergen doses given by nebulisation through the mouth. No more than a 5% fall in forced expiratory volume in one second. Nasal allergen challenge: One drop of increasing allergen doses on nasal mucosa.
Primary Outcome Measure Information:
Title
Change in CysLT1-r following allergen challenge
Time Frame
At 7h and 24h following conventional challenge
Secondary Outcome Measure Information:
Title
Change in CysLT1-r following low dose allergen challenge
Time Frame
At 2 and 4 days of challenge
Title
Difference in CysLT1-r expression in asthma and allergic rhinitis
Time Frame
At baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: To have a positive reaction to one or more allergen on prick tests. Non smokers No respiratory track infection for at least one month prior to the study. Asthmatic subjects using only inhaled beta-2 agonists on an as needed basis for their asthma treatment. Asthmatic subjects with a history of asthma of at least 6 months. Asthmatic subjects with PC20 methacholine lower or equal to 8 mg/ml. Allergic rhinitic subjects never experienced any asthma symptoms or took any asthma medication in the past. Allergic rhinitic subjects with a PC20 methacholine higher than 16 mg/ml. Exclusion Criteria: Smokers or ex smokers less than 6 months or more than 10 pack-years. Asthmatic subjects using or used in the past 3 months inhaled or oral corticosteroids.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie-Eve Boulay, MSc
Phone
418-656-8711
Ext
2617
Email
Marie-Eve.Boulay@crhl.ulaval.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Philippe Prince, MSc
Phone
418-656-8711
Ext
2672
Email
Philippe.Prince@crhl.ulaval.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis-Philippe Boulet, MD
Organizational Affiliation
Hopital Laval
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre de recherche de l'Hopital Laval
City
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Individual Site Status
Recruiting

12. IPD Sharing Statement

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CysLT1-r Expression Following Allergen Exposure in Asthma and Allergic Rhinitis

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