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2004 SEP 20 - (NewsRx.com & NewsRx.net) -- NexMed, Inc., (NASDAQ:NEXM) announced that it will present the new findings of a pilot clinical study conducted offshore, entitled "A Pilot Clinical Study of a Topical Alprostadil Cream for the Treatment of Female Sexual Arousal Disorder (FSAD)."
The presentation will take place at the Annual Meeting of the International Society for the Study of Women's Sexual Health on October 28-31, 2004, in Atlanta, Georgia. Femprox is NexMed's proprietary FSAD treatment under development and incorporates alprostadil (PGE) with the patented NexACT technology.
This was a randomized, placebo-controlled, double-blind, crossover clinical study that tested eight female patients, 21-45 years of age, diagnosed with FSAD (as defined by their sexual history, Female Sexual Distress Scale, and psychological assessment) for more than 6 months. The subjects received both a placebo cream and Femprox.
The primary efficacy end point was measured as the score of the arousal success or the number of the "Yes" responses to question 3 of the female sexual encounter ...