Female Sexual Arousal Disorder, Positive Femprox Study Results
The patients, who were between the ages of 21 and 65, were randomly assigned to placebo or one of three strengths of Femprox. They were required to use one application of Femprox prior to engaging in sexual activity, up to ten times during two treatment evaluation periods. The primary efficacy end point was the arousal success rate determined by the internationally recognized Female Sexual Encounter Profile (FSEP) questionnaire. Secondary efficacy end points included changes in the Female Sexual Function Index (FSFI), in other FSEP responses, and in the Female Sexual Distress Scale (FSDS), as well as the Global Assessment Question (GAQ).
The primary efficacy endpoint was statistically significant at the end of both evaluation periods. Patients showed demonstrable improvement in sexual arousal over the course of therapy. At the end of the first evaluation period, 17% and 38.7% (p
Femeie sexual Arousal tulburare, rezultatele pozitive Femprox - Female Sexual Arousal Disorder, Positive Femprox Study Results - articole medicale engleza - startsanatate