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Completed

NCT Number: NCT05113615

Regular Use Tiotropium and Tolerance to Bronchoprotection in Mild Asthma

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Asthma Research Lab University of Saskatchewan Room 346 Ellis Hall

Saskatoon, Saskatchewan, S7N 0W8, Canada

About this study

A single dose of an inhaled muscarinic antagonist will protect against methacholine induced bronchoconstriction and increase the dose of methacholine required to cause bronchoconstriction about 4 doubling doses. Beta agonist bronchodilators also shift the dose response curve to the right but the protection against methacholine induced bronchoconstriction is lost (i.e. tolerance develops) with regular use. This study will determine if bronchoprotection is lost following regular use of tiotropium.

This will be a randomized, double-blind placebo controlled study to assess the development of tolerance following regular use of tiotroium in a population of mild asthmatics.

Tiotropium will be administered at the clinically recommended dose (5mcg/day) for a total of 8 days. Methacholine challenges will be performed at baseline (pre-treatment), at one hour post first dose and on day 8, one hour after the final dose. The same will dosing schedule and assessments will occur with an identical placebo inhaler.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Tiotropium Bromide

Drug

respimat inhaler 2.5mcg/puff

Other names: Spiriva Respimat

Matching Placebo

Drug

matching placebo Respimat inhaler

Primary outcomes

  1. Methacholine PD20

    Time frame: pre treatment

    dose of methacholine required to induce a 20% fall in FEV1 (volume of air forcefully exhaled in the first second following a full inhalation)

  2. Methacholine PD20

    Time frame: one hour post first dose

    dose of methacholine required to induce a 20% fall in FEV1 (volume of air forcefully exhaled in the first second following a full inhalation)

  3. Methacholine PD20

    Time frame: one hours post final dose

    dose of methacholine required to induce a 20% fall in FEV1 (volume of air forcefully exhaled in the first second following a full inhalation)

Sponsors and collaborators

Lead sponsor

University of Saskatchewan

Other

Registry information

Official study title

Daily Dosing of Tiotropium and Tolerance to Bronchoprotection Against Methacholine Challenge

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Nov 9, 2021
Registry last updated
May 23, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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