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Tolerance 3

The effects of repeated bronchoconstriction on response to "reliever" medication in asthma.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000353695
Enrollment
12
Registered
2005-09-09
Start date
2004-01-02
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Randomised, placebo-controlled, cross-over investigation. There will be two phases during which beta agonist will or will not be given on a regular basis. Each phase will last a month, with a 1-2 week washout period inbetween. At each visit, 2 bronchial challenges will be administered and either placebo, anti-cholinergic or beta-agonist relief will be given.

Sponsors

Otago Medical Research Foundation
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
12 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Asthma (according to the ATS), Non-smokers.

Exclusion criteria

Pregnancy, high dose ICS, history of life-threatening asthma, unable to tolerate ipratropium as a reliever inhaler, recent use of oral steroids, LRTI.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026