drugset / Trial / NCT00118495
Zestra in Women With Mixed Sexual Dysfunction
RandomizedParallel-groupDouble-blindTreatment
Summary
The objective of this study is to evaluate the clinical efficacy and safety of Zestra(TM) in women with acquired mixed desire/interest/arousal/orgasm disorders under conditions of home usage. The primary efficacy hypothesis will compare the effect of Zestra versus placebo on the incidence of "successful and satisfactory" sexual encounters.
Timeline
- Start
- 2006-03
- Primary completion
- —
- Completion
- 2007-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Zestra(TM) | Unknown | — | — |