Ignite Creation Date:
2024-05-05 @ 5:25 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00452348
Status:
COMPLETED
Last Update Posted:
2016-12-09
First Post:
2007-03-26
Brief Title:
A 12-Month Study Comparing Fluticasone PropionateSalmeterol ADVAIR DISKUS Combination Product 25050mcg Twice Daily To Fluticasone Propionate FLOVENT DISKUS 250 mcg Twice Daily In Symptomatic Patients With Asthma
Sponsor:
Organization:
GlaxoSmithKline
Study Design
Study Type:
INTERVENTIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
None
Target Duration:
None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
None
Bio Spec Description:
None
Enrollment Count:
628
Enrollment Type:
ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
| Name |
|---|
| PHASE4 |
Observational Models:
Time Perspective List:
Who Masked List: