Background Erectile dysfunction is a common medical problemaffecting many men. Although several intracavernosal therapiesare available, their efficacy and safety have not been studiedsystematically.
Methods We investigated the efficacy and safety of alprostadilformulated for intracavernosal treatment in three separate multi-institutional,prospective studies in men with erectile dysfunction of vasculogenic,neurogenic, psychogenic, and mixed causes. Clinical and laboratoryevaluations of erection and the feasibility and satisfactorinessof sexual activity as assessed both by the men and by theirpartners were the primary measures of efficacy.
Results In a doseresponse study of 296 men, all dosesof alprostadil were superior to placebo and there was a significantdoseresponse relation (P<0.001), resulting in higherresponse rates with increasing doses of alprostadil (from 2.5to 20 µg). In a dose-finding study of 201 men, the minimaleffective dose was <2 µg in 23, 20, 38, and 23 percentof men with erectile dysfunction of neurogenic, vasculogenic,psychogenic, or mixed causes, respectively. In a six-month self-injectionstudy in 683 men, the participants reported being able to havesexual activity after 94 percent of the injections. The menand their partners rated the sexual activity as satisfactoryafter 87 and 86 percent of the injections, respectively. Penilepain, usually mild, occurred in 50 percent of the men at sometime but after only 11 percent of the injections. Prolongederections occurred in 5 percent of the men, priapism in 1 percent,penile fibrotic complications in 2 percent, and hematoma orecchymosis in 8 percent.
Conclusions In men with erectile dysfunction, intracavernosalinjection of alprostadil is an effective therapy with tolerableside effects.
Source Information
From the Clinical Development Unit, the Upjohn Company, Kalamazoo, Mich.
Address reprint requests to Dr. Linet at the Upjohn Company, 7000 Portage Rd., Kalamazoo, MI 49001-0199.
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