1. Silodosin versus naftopidil in the treatment of premature ejaculation: A prospective multicenter trial
- Author
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Musashi Tobe, Toshikazu Otani, Yoshikazu Sato, Kazunori Haga, Toshiyasu Amano, Nobuyuki Kondou, Tohru Araki, Ichiya Honma, Masanori Matsukawa, and Kousuke Uchida
- Subjects
Adult ,Male ,medicine.medical_specialty ,Indoles ,Time Factors ,Ejaculation ,Urology ,030232 urology & nephrology ,Self Administration ,Naphthalenes ,Piperazines ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Multicenter trial ,Premature ejaculation ,medicine ,Humans ,Prospective Studies ,Premature Ejaculation ,Aged ,030219 obstetrics & reproductive medicine ,Naftopidil ,business.industry ,Silodosin ,Middle Aged ,medicine.disease ,Erectile dysfunction ,Treatment Outcome ,Clinical Global Impression ,Adrenergic alpha-1 Receptor Antagonists ,Urological Agents ,Intravaginal ejaculation latency time ,medicine.symptom ,business ,medicine.drug - Abstract
Objectives To determine the efficacy of two α1-adrenoceptor antagonists with different affinities for α1-adrenoceptor subtypes, silodosin and naftopidil, in the treatment of premature ejaculation. Methods This was a prospective, open-label, multicenter trial. A total of 26 patients with untreated acquired premature ejaculation were enrolled. Premature ejaculation was defined based on the International Society for Sexual Medicine recommendation. Patients self-administered on demand silodosin 4 mg or naftopidil 25 mg 1 h before intercourse, alternating drugs at least three times each. Clinical global impression change for premature ejaculation, premature ejaculation profile, and intravaginal ejaculation latency time were evaluated at baseline and during treatment. Results Due to clinical global impression change, 24 patients (92%) and 12 patients (46%) reported improvement in their own premature ejaculation problems under silodosin and nafitopidil administration, respectively. Silodosin treatment produced a significantly higher improvement rate compared with naftopidil (P = 0.0002). Objectively, silodosin significantly prolonged intravaginal ejaculation latency time compared with baseline and naftopidil (P < 0.01). Mean intravaginal ejaculation latency times were 1.9, 4.1, and 7.6 min at baseline, control and with silodosin, respectively. The rate of reduced semen volume during silodosin treatment was higher than during naftopidil treatment. There were no adverse systemic effects in either group. Conclusions Silodosin, a highly selective α1A-adrenoceptor antagonist, produces greater improvements in premature ejaculation profiles and related symptoms along with intravaginal ejaculation latency time in acquired premature ejaculation patients with or without erectile dysfunction. This result supports the clinical use of silodosin as an alternative treatment for premature ejaculation.
- Published
- 2016