drugset / Trial / NCT00117325
Study Of Adults And Adolescents With Vasomotor Rhinitis
RandomizedParallel-groupTreatment
Summary
The primary objective of this study is to compare the efficacy and safety of GW685698X 100mcg once daily (QD) aqueous nasal spray with vehicle placebo nasal spray in adult and adolescent subjects (12 years of age and older) with vasomotor rhinitis (VMR).
Timeline
- Start
- 2005-07-11
- Primary completion
- 2006-02-09
- Completion
- 2006-02-09
Outcome
Missed primary endpoint
registry analysis (superiority or other test); Placebo vs Fluticasone Furoate 110 mcg QD; p = 0.050; Mean Difference (Net) -0.335 (95% CI -0.67 to 0.00); ANCOVA NCT00117325 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fluticasone Furoate | Other / unclassified | 100 ug | Intranasal |