Last updated: 11/07/2018 18:50:59
A randomised, double blind, parallel group comparison of the effect of the salmeterol/fluticasone propionate combination product (50/250 mcg strength) bd via the Diskus inhaler with placebo bd via the Diskus inhaler in young adults who are in clinical remission of allergic 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 randomised, double blind, parallel group comparison of the effect of the salmeterol/fluticasone propionate combination product (50/250 mcg strength) bd via the Diskus inhaler with placebo bd via the Diskus inhaler in young adults who are in clinical remission of allergic asthma
Trial description: A randomised, double blind, parallel group comparison of the effect of the salmeterol/fluticasone propionate combination product (50/250 mcg strength) bd via the Diskus inhaler with placebo bd via the Diskus inhaler in young adults who are in clinical remission of allergic 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:
Van Den Toorn LM, Prins JB, de Jongste JC, et al. Benefit from anti-inflammatory treatment during clinical remission of atopic asthma. Respiratory Medicine 2005; 99 (6): 779-787.
Van den Toorn LM, Prins JB, De Jongste JC, Leman K, Mulder PG, Hoogsteden HC et al. Benefit from anti-inflammatory treatment during clinical remission of atopic asthma. Respir Med 2005; 99(6):779-87
Medical condition
Asthma
Product
fluticasone propionate/salmeterol
Collaborators
Not applicable
Study date(s)
June 1999 to April 2001
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
2001-01-04
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
Participate in clinical trial
Access to clinical trial data by researchers
Visit website