Status:

COMPLETED

Methacholine Challenge: Comparison of Doubling and Quadrupling Methacholine Dose Regimes Using the Tidal Volume Method

Lead Sponsor:

University of Saskatchewan

Conditions:

Asthma

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to determine the difference (if any) in the result of the methacholine challenge (a test used by physicians in diagnosing asthma) when concentrations of methacholine are q...

Detailed Description

The purpose of this study is to confirm that the tidal volume technique of methacholine delivery may be employed in methacholine challenges using a quadrupling dose schedule instead of the standard do...

Eligibility Criteria

Inclusion

  • You must be over 18 years of age; and
  • You must have a diagnosis of asthma; and
  • Excluding asthma, you are not aware of any other lung conditions or diseases.

Exclusion

  • You have a known hypersensitivity (i.e. an overreaction of your immune system) to methacholine or other parasympathomimetic agents or cholinesterase inhibitors (i.e. agents that act in a similar way via your nervous system - to be discussed with study personnel); or
  • You are a nursing mother or if you are a woman of child bearing potential who is, may be, or intends to become pregnant during testing as the effects of methacholine inhalation in these situations are not known; or
  • Your baseline lung function is poor (ie. your FEV or forced expiratory volume in one second, is less than 65% of your predicted values). This will be performed and explained by study personnel prior to commencing methacholine inhalation testing; or
  • You have had any respiratory infections for the last four weeks; or
  • If you have allergies, and have been exposed to agents that trigger your asthma within the last four weeks; or
  • If you have any significant chronic medical condition.

Key Trial Info

Start Date :

February 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 1 2009

Estimated Enrollment :

15 Patients enrolled

Trial Details

Trial ID

NCT00890539

Start Date

February 1 2009

End Date

March 1 2009

Last Update

November 25 2009

Active Locations (1)

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1

University of Saskatchewan

Saskatoon, Saskatchewan, Canada, S7N 0W8