drugset / Trial / NCT00696787
A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate if DVS SR is safe and effective in the treatment of pain associated with fibromyalgia syndrome, and if so to identify the efficacious doses.
Timeline
- Start
- 2008-06
- Primary completion
- 2009-01
- Completion
- 2009-01
Outcome
Missed primary endpoint
registry analysis (superiority or other test); Placebo vs DVS SR; p = 0.471; Adjusted mean -0.38 (95% CI -1.42 to 0.66); ANCOVA NCT00696787 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Desvenlafaxine | Other / unclassified | 200 mg | — |
| Comparator | Pregabalin | Small molecule | 450 mg | — |