Last updated: 11/07/2018 18:39:00
A multi-centre, randomised, double-blind, placebo-controlled parallel group study to compare the effect on airway inflammation and remodeling of treatment with salmeterol/fluticasone propionate combination product (50/100mg strength) bd via the Accuhaler inhaler, or fluticasone propionate…
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 multi-centre, randomised, double-blind, placebo-controlled parallel group study to compare the effect on airway inflammation and remodeling of treatment with salmeterol/fluticasone propionate combination product (50/100mg strength) bd via the Accuhaler inhaler, or fluticasone propionate…
Trial description: A multi-centre, randomised, double-blind, placebo-controlled parallel group study to compare the effect on airway inflammation and remodeling of treatment with salmeterol/fluticasone propionate combination product (50/100mg strength) bd via the Accuhaler inhaler, or fluticasone propionate…
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:
Beckett P, Hewitt L, Woodcock A, Smith J, Seghal N, Rice L, Chopra N, Howarth P. Improvement in airway hyper-responsiveness (AHR) and lung function with salmeterol/fluticasone propionate combination (SFC) in persistent asthma. Am J Resp & Crit Care Med 2003; 167; supp 7: A890
Howarth P, Hewitt L, Woodcock A, Rice L, Whitehead C, Smith J . Salmeterol/fluticasone propionate combination (SFC) improves airways hyper-responsiveness (AHR), lung function and symptoms in adult patients with mild asthma. ERJ 2004; 24; supp 48: 262s (P1715)
Medical condition
Asthma
Product
fluticasone propionate/salmeterol
Collaborators
Not applicable
Study date(s)
June 2000 to February 2003
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
2003-25-02
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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