NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000000839

Registered date:01/10/2007

Randomized, double-blind, placebo-controlled crossover study of ejaculatory disorder caused by orally administered silodosin in healty volunteer men

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedJapanese healthy volunteer men
Date of first enrollment2007/10/01
Target sample size50
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Silodosin (Wash-out) Placebo Placebo (Wash-out) Silodosin

Outcome(s)

Primary OutcomeNumerical Rating Scale(NRS)
Secondary Outcome

Key inclusion & exclusion criteria

Age minimumNot applicable
Age maximumNot applicable
GenderMale
Include criteria
Exclude criteriaMen who are taking alpha adrenergic receptor blockade Men who have received transurethral resection of prostate (TUR-P) Men who have retrograde ejaculation Men who have received retroperitoneal lymph node dissection (RPLND) Men who have been diagnosed erectile dysfunction (ED) Men who have been diagnosed diabetes

Related Information

Contact

public contact
Name Fumitaka Shimizu
Address Japan
Telephone
E-mail fshimizu-jua@umin.ac.jp
Affiliation Graduate school of medicine, Juntendo University Department of Urology
scientific contact
Name Fumitaka Shimizu
Address 2-1-1, Hongo, Bunkyo-ku, Tokyo,113-8421 Japan Japan
Telephone 03-5802-1227
E-mail
Affiliation Graduate school of medicine, Juntendo University Department of Urology