Last updated: 11/07/2018 17:04:11
A Multi-centre, Randomised, Double-Blind, Parallel-Group Study to Compare the Efficacy and Safety of Fluticasone Propionate 100?g bd (200?g Daily) Produced by Two Recrystallisation Processes (“Old Process” “New Process”) Administered Via Dry Powder Inhaler, and With “New Process” Fluticasone Pro ...
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, Parallel-Group Study to Compare the Efficacy and Safety of Fluticasone Propionate 100?g bd (200?g Daily) Produced by Two Recrystallisation Processes (“Old Process” “New Process”) Administered Via Dry Powder Inhaler, and With “New Process” Fluticasone Pro ...
Trial description: A Multi-centre, Randomised, Double-Blind, Parallel-Group Study to Compare the Efficacy and Safety of Fluticasone Propionate 100?g bd (200?g Daily) Produced by Two Recrystallisation Processes (“Old Process” “New Process”) Administered Via Dry Powder Inhaler, and With “New Process” Fluticasone Pro ...
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:
Dahl R. The safety and efficacy of fluticasone propionate 200mcg daily given via the Diskhaler inhaler as compared with the pressurised metered dose inhaler in adult asthma. Clinical and Experimental Allergy 1993; 23(Suppl. 1): 81.
Medical condition
Asthma
Product
fluticasone propionate
Collaborators
Not applicable
Study date(s)
February 1991 to December 1992
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
1992-18-12
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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