Last updated: 11/07/2018 19:21:44
A multicenter, randomized, double-blind, parallel-group trial to evaluate the long-term efficacy and safety of inhaled salmeterol 50mg BID compared to short-acting b2-agonists as-needed in adult patients with asthma.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A multicenter, randomized, double-blind, parallel-group trial to evaluate the long-term efficacy and safety of inhaled salmeterol 50mg BID compared to short-acting b2-agonists as-needed in adult patients with asthma.
Trial description: A multicenter, randomized, double-blind, parallel-group trial to evaluate the long-term efficacy and safety of inhaled salmeterol 50mg BID compared to short-acting b2-agonists as-needed in adult patients with asthma.
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:
DUrzo AD, Chapman KR, Cartier A, Hargreave FE, Fitzgerald M, Tesarowski D. Effectiveness and safety of salmeterol in nonspecialist practice settings. Chest 2001; 119:714-719.
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
1996-30-10
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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