Last updated: 11/07/2018 19:16:34
A multicentre, randomised, double-blind, double-dummy, parallel-group, three-month comparison of the salmeterol/fluticasone propionate combination product (2x25/250mcg strength) bd via the pressurised metered dose inhaler with salmeterol/fluticasone propionate combination product (1x50/500mcg st ...
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 multicentre, randomised, double-blind, double-dummy, parallel-group, three-month comparison of the salmeterol/fluticasone propionate combination product (2x25/250mcg strength) bd via the pressurised metered dose inhaler with salmeterol/fluticasone propionate combination product (1x50/500mcg st ...
Trial description: A multicentre, randomised, double-blind, double-dummy, parallel-group, three-month comparison of the salmeterol/fluticasone propionate combination product (2x25/250mcg strength) bd via the pressurised metered dose inhaler with salmeterol/fluticasone propionate combination product (1x50/500mcg st ...
Primary purpose:
Not applicable
Trial design:
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Masking:
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Allocation:
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Primary outcomes:
Not applicable
Secondary outcomes:
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Interventions:
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Enrollment:
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Primary completion date:
Not applicable
Observational study model:
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Time perspective:
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Clinical publications:
Abstract: Benefits of fluticasone propionates/salmeterol hfa mdi are apparent on the first day of dosing. O'Brien, J, Carlos-Palma, A, Bogolubov, M, Davies, P, and Payne, E American Lung Association/American Thoracic Society 97th International Conference 5/18/2001 San Francisco CA
Abstract: Clinical equivalence of salmeterol/fluticasone propionate combination 5/500 bid delivered via metered dose inhaler (mdi) or diskus in patients with reversible airways obstruction. van Noord, J A MD, Lill, H MD, Carillo, T MD, and Davies, P MD American Lung Association/American Thoracic Society 96th International Conference 5/5/2000
Abstract: Clinical equivalence of salmeterol/fluticasone propionate combination product (seretide) 50/500mcg bd delivered via diskus or cfc-free metred dose inhaler (mdi) in patients with reversible airways obstruction. Davies, P, Van Noord, J A, Lill, H, Carillo, T, and Greefhorst, A P 19th Congress of the European Academy of Allergology and Clinical Immunology (EAACI) 7/1/2000 Lisbon Portugal
Abstract: Comparative effectiveness of salmeterol/fluticasone propionate combination 50/500 bid delivered via metered dose inhaler or diskus in patients with reversible airways obstruction. van Noord, J A MD, Carillo, T MD, Lill, H MD, and Davies, P MD American Academy of Allergy, Asthma and Immunology 56th Annual Meeting 3/3/2000 San Diego CA
Davies P, van Noord JA, Lill H, Carrillo T, Greefhorst AP. Clinical equivalence of salmeterol/fluticasone propionate combination product (Seretide/Advair) 50/500 mcg bd delivered via Diskus or CFC-free metered dose inhaler (MDI) in patients with reversible airways obstruction. Eur J Allergy & Clin Immunol; 2000; 55 (Suppl 63): 16
O’Brien J, Carlos-Palma A, Bogolubov M, Davies P, Payne E. Benefits of fluticasone propionate/salmeterol (Advair/Seretide/Advair) HFA MDI are apparent on the first day of dosing. Am J Respir Crit Care Med 2001; 163 (5 part 2): A864
van Noord JA, Lill H, Carillo T, Davies P. Comparative effectiveness of salmeterol/fluticasone propionate combination 50/500 bid delivered via metered dose inhaler or Diskus in patients with reversible airways obstruction. J Allergy Clin Immunol 2000; 105 (1 part 2): S15 (45)
van Noord JA, Lill H, Carrillo Diaz T, Greefhorst AP, Davies P. Clinical equivalence of salmeterol/fluticasone propionate combination product (50/500?g) delivered via a chlorofluorocarbon-free metered dose inhaler with the Diskus in patients with moderate to severe asthma. Clin Drug Invest 2001: 21 (4): 243-255
van Noord JA, Lill H, Carrillo T, Davies P. Clinical equivalence of salmeterol/fluticasone propionate combination 50/500 bid delivered via metered dose inhaler (MDI) or Diskus in patients with reversible airways obstruction. Am J Respir Crit Care Med 2000; 161 (3 part 2 Suppl 1): A197
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
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Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1999-16-03
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
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