Evaluating the Impact of Single Dose Tiotropium on Allergen-induced Early Asthmatic Response

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Saskatchewan

About this trial

Evaluate single dose (2 x 2.5mcg/puff; total dose 5mcg) effect of tiotropium administered 30 minutes prior to allergen challenge on allergen-induced EAR assessed as the maximal % fall in FEV1 after allergen inhalation compared to that of single dose (two puffs) matched placebo administered 30 minutes prior to allergen challenge.

Eligibility criteria

Qualifiers

age (years) at least 18 years

no confounding health issue (i.e. no health conditions, other than asthma, that would put the participant at risk or affect data integrity as determined by the principal investigator)

baseline FEV1 ≥ 65% of predicted normal at Visit 1

evidence of atopy to an allergen suitable for inhalation challenge following skin prick testing such as house dust mite, grass, cat or horse

Disqualifiers

Smoker >10 pack year history

Trial design

Treatments tested in this trial

  • Tiotropium (Spiriva®)
  • Placebo

Treatment groups

10 Participants
are divided into 2 treatment groups

Sponsors and collaborators