Last updated:  11/06/2018 23:32:40
A 24-week randomized, double-blind, multicenter study to compare safety, efficacy and tolerability of modified release Avandia (8mg OD) and immediate release Avandia (8mg OD) in patients with type 2 diabetes mellitus
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 24-week randomized, double-blind, multicenter study to compare safety, efficacy and tolerability of modified release Avandia (8mg OD) and immediate release Avandia (8mg OD) in patients with type 2 diabetes mellitus
Trial description: A 24-week randomized, double-blind, multicenter study to compare safety, efficacy and tolerability of modified release Avandia (8mg OD) and immediate release Avandia (8mg OD) in patients with type 2 diabetes mellitus
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:
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Clinical study report
Available language(s): English
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
2005-07-06
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