Overview

Regular Use Tiotropium and Tolerance to Bronchoprotection in Mild Asthma

Status:
Not yet recruiting
Trial end date:
2022-04-01
Target enrollment:
0
Participant gender:
All
Summary
The study will assess if regular use of tiotropium (i.e. daily) results in loss of bronchoprotection against methacholine induced bronchoconstriction in those with mild asthma.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Saskatchewan
Treatments:
Bromides
Tiotropium Bromide
Criteria
Inclusion Criteria:

- diagnosis of asthma

- asthma is currently well controlled using only occasional bronchodilators

- baseline lung function (FEV1) is greater than 65% of the predicted value

- exhibit bronchoconstriction to inhaled methacholine at a dose of 200mcg or less

Exclusion Criteria:

- women who are pregnant or breastfeeding.

- diagnosis of another lung condition or medical condition that would pose a risk to the
participant if enrolled in the study

- current smokers of nicotine products (e.g., cigarettes).

- users of cannabis or other inhaled recreational products (e.g., e-cigarettes or other
vaping products) on a daily basis

- respiratory infection within 4 weeks of entering the study

- use of any anticholinergic agent within 30 days prior to the beginning of the study
(e.g., ipratropium or the study treatment tiotropium).

- known hypersensitivity to tiotropium bromide or components of tiotropium formulation
(e.g., benzalkonium chloride), to atropine or its derivatives.