Last updated: 11/07/2018 19:26:22
A 12 week study to compare the efficacy and safety of salmeterol xinafoate plus beclomethasone dipropionate with a double dose of beclomethasone dipropionate in patients with mild to moderate reversible airways obstruction treated by a general practitioner.
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 12 week study to compare the efficacy and safety of salmeterol xinafoate plus beclomethasone dipropionate with a double dose of beclomethasone dipropionate in patients with mild to moderate reversible airways obstruction treated by a general practitioner.
Trial description: A 12 week study to compare the efficacy and safety of salmeterol xinafoate plus beclomethasone dipropionate with a double dose of beclomethasone dipropionate in patients with mild to moderate reversible airways obstruction treated by a general practitioner.
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:
Vermetten FAAM, Boermans AJM, Luiten WDVF et al. Comparison of salmeterol with beclomethasone in adult patients with mild persistent asthma who are already on low-dose inhaled steroids. J Asthma. 1999; 36: 97- 106.
Medical condition
Airway Obstruction
Product
salmeterol
Collaborators
Not applicable
Study date(s)
January 1993 to July 1995
Type
Not applicable
Phase
3
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
1995-01-07
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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