drugset / Trial / NCT00102882
Study Of Asthma And Genetics In Patients To Be Treated With Fluticasone Propionate/Salmeterol Or Salmeterol Xinafoate
RandomizedParallel-groupDouble-blindTreatment
Summary
This study may last up to 36-38 weeks. Patients will visit the clinic 11 times. A blood sample will be taken at Visit 1 to look at subjects' genes. Breathing tests will be done during the study. Study medicines and procedures will be provided at no cost. Patients will be treated with VENTOLIN (8 wks), ATROVENT (8 wks), then ADVAIR or SEREVENT (16 wks). ADVAIR and SEREVENT are FDA approved for the treatment of asthma in patients 4 years of age and older.
Timeline
- Start
- 2004-10
- Primary completion
- 2007-01
- Completion
- 2007-01
Outcome
Missed primary endpoint
paper no statistically significant changes from baseline between genotypes within treatments were observed. PMID 19910613 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fluticasone propionate | Other / unclassified | 100 ug | — |
| Subject | Salmeterol | Other / unclassified | 50 ug | — |