None listed
Conditions
Interventions
A single dose of inhaled tiotropium bromide with measurement of FEV1 over the following 24 hours. Then a 7 day 'washout' period follwed by cross-over to the alternate study arm and repeat
Sponsors
Mater Adults Hospital, South Brisbane
Study design
Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
Confirmed CF, stable disease ( no infective exacerbation for prior 2 weeks ).
Exclusion criteria
Recent infective exacerbation in prior 2 weeks, pregnant/breastfeeding.
Outcome results
None listed