Last updated: 11/07/2018 19:21:57
A 12 week randomized, double-blind, parallel group study evaluating effect of salmeterol 50mcg BID or fluticasone propionate 100mcg BID for control of airway inflammation in subjects with asthma, when added to current inhaled corticosteroid therapy.
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A 12 week randomized, double-blind, parallel group study evaluating effect of salmeterol 50mcg BID or fluticasone propionate 100mcg BID for control of airway inflammation in subjects with asthma, when added to current inhaled corticosteroid therapy.
Trial description: A 12 week randomized, double-blind, parallel group study evaluating effect of salmeterol 50mcg BID or fluticasone propionate 100mcg BID for control of airway inflammation in subjects with asthma, when added to current inhaled corticosteroid therapy.
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:
Li X, Ward C, Thien F, et al. An anti-inflammatory effect of salmeterol, a long-acting ?2-agonist, assessed in airway biopsies and bronchoalveolar lavage in asthma. Am J Respir Crit Care Med 1999;160:1493-1499
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
1996-30-11
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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