Last updated: 11/07/2018 19:26:49
Inhaled salmeterol in adolescents and adult patients with mild to moderate chronic reversible obstructive airways disease. A multicenter, randomized, double-blind, parallel, comparative clinic trial of twelve week courses of 50µg salmeterol administered twice daily, versus 200µg salbutamol admi ...
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Inhaled salmeterol in adolescents and adult patients with mild to moderate chronic reversible obstructive airways disease. A multicenter, randomized, double-blind, parallel, comparative clinic trial of twelve week courses of 50µg salmeterol administered twice daily, versus 200µg salbutamol admi ...
Trial description: Inhaled salmeterol in adolescents and adult patients with mild to moderate chronic reversible obstructive airways disease. A multicenter, randomized, double-blind, parallel, comparative clinic trial of twelve week courses of 50µg salmeterol administered twice daily, versus 200µg salbutamol admi ...
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Boulet LP, Laviolette M, Boucher S, et al. A twelve-week comparison of salmeterol and salbutamol in the treatment of mild-to-moderate asthma: a Canadian multicentre study. J Allergy Clin Immunol 1997; (99): 13-21.
Medical condition
Airway Obstruction
Product
salmeterol
Collaborators
Not applicable
Study date(s)
January 1991 to February 1992
Type
Not applicable
Phase
4
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1992-18-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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