Last updated: 11/07/2018 18:40:48
A Danish, multi-centre, comparative, parallel-group study to determine whether initiation of combination treatment with Seretide™ 50/100 mg bd offers better asthma control than monotherapy with Flixotide™ 100 mg bd to adult asthmatic subjects uncontrolled on short-acting bronchodilator alone.
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 Danish, multi-centre, comparative, parallel-group study to determine whether initiation of combination treatment with Seretide™ 50/100 mg bd offers better asthma control than monotherapy with Flixotide™ 100 mg bd to adult asthmatic subjects uncontrolled on short-acting bronchodilator alone.
Trial description: A Danish, multi-centre, comparative, parallel-group study to determine whether initiation of combination treatment with Seretide™ 50/100 mg bd offers better asthma control than monotherapy with Flixotide™ 100 mg bd to adult asthmatic subjects uncontrolled on short-acting bronchodilator alone.
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:
Strand AM & Luckow A: Initiation of maintenance treatment of persistent asthma: salmeterol/fluticasone propionate. Respiratory Medicine 2004, 98: 1008-1015
Strand AM & Luckow A: Initiation of treatment with salmeterol/fluticasone propionate combination product is more effective than inhaled steroid alone in asthmatic patients symptomatic on short-acting bronchodilator alone, ERS 2003
Medical condition
Asthma
Product
fluticasone propionate/salmeterol
Collaborators
Not applicable
Study date(s)
April 2001 to Invalid Date
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
Not applicable
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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