NCT lookup
Pull any trial record directly from ClinicalTrials.gov.
Reversibility of Methacholine Induced Bronchoconstriction
Reversibility of Methacholine Induced Bronchoconstriction
CompletedPhase 4
Sponsor: University of Saskatchewan
Conditions: Asthma
Interventions: salbutamol aqueous solution, salbutamol pressurized metered dose inhaler, placebo
Countries: Canada
The study will compare salbutamol reversibility of methacholine induced bronchoconstriction between a pressurized metered dose inhaler with a spacer versus nebulizer administration using a vibrating mesh nebulizer.
Eligibility overview
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * age (years) at least 18, male or female * no confounding health issue (i.e. no health conditions, other than asthma, that would put the participant at risk or affect data integrity) * baseline FEV1 ≥ 65% predicted (per Quanjer GLI 2012) * methacholine PD20 ≤ 800mcg Exclusion Criteria: * respiratory infection within 4 weeks of Visit 1 * exposure to triggers of respiratory symptoms within 4 weeks of Visit 1 * currently pregnant or breastfeeding * current smoker (cigarettes, vaping)
Locations (1)
- Saskatoon, Saskatchewan, Canada