TY - JOUR
T1 - Efficacy and safety of on-demand oral tadalafil in the treatment of men with erectile dysfunction in Taiwan
T2 - A randomized, double-blind, parallel, placebo-controlled clinical study
AU - Chen, Kuang Kuo
AU - Jiann, Bang Ping
AU - Lin, Johnny Shinn Nan
AU - Lee, Shang Sen
AU - Huang, Shih Tsung
AU - Wang, Chii Jye
AU - Hsie, Ju Ton
AU - Su, Chung Kuang
AU - Costigan, Timothy M.
AU - Emmick, Jeffrey T.
PY - 2004
Y1 - 2004
N2 - Introduction. Tadalafil is a phosphodiesterase type 5 inhibitor for the treatment of erectile dysfunction (ED). Past clinical trials have assessed its efficacy and safety in western populations. Tadalafil has not been investigated in a large clinical trial with a South-east Asian population. Aim. To assess the efficacy and safety of on-demand tadalafil for the treatment of ED in a 12-week, double-blind, placebo-controlled study in Taiwan. Methods. Men with mild to severe ED of various etiologies were randomized to receive placebo, tadalafil 10 mg, or tadalafil 20 mg, taken as needed (maximum once daily). Efficacy assessments included the International Index of Erectile Function, the Sexual Encounter Profile (SEP) diary, and a Global Assessment Question (GAQ). Results. Tadalafil significantly improved erectile function compared with placebo (P < 0.005, all measures). At endpoint, the patients receiving tadalafil reported a greater mean per-patient percentage of successful intercourse attempts (SEP question 3: 70.0%, 10 mg; 78.0%, 20 mg) than placebo-treated patients (42.8%) and a greater proportion of improved erections (GAQ: 92.3% and 84.6% vs. 54.5%). Most treatment-emergent adverse events were mild or moderate. The most common adverse events were back pain, dyspepsia, and myalgia. Conclusions. Tadalafil was an effective, well-tolerated therapy for men in Taiwan with ED of broad-spectrum severity and etiology.
AB - Introduction. Tadalafil is a phosphodiesterase type 5 inhibitor for the treatment of erectile dysfunction (ED). Past clinical trials have assessed its efficacy and safety in western populations. Tadalafil has not been investigated in a large clinical trial with a South-east Asian population. Aim. To assess the efficacy and safety of on-demand tadalafil for the treatment of ED in a 12-week, double-blind, placebo-controlled study in Taiwan. Methods. Men with mild to severe ED of various etiologies were randomized to receive placebo, tadalafil 10 mg, or tadalafil 20 mg, taken as needed (maximum once daily). Efficacy assessments included the International Index of Erectile Function, the Sexual Encounter Profile (SEP) diary, and a Global Assessment Question (GAQ). Results. Tadalafil significantly improved erectile function compared with placebo (P < 0.005, all measures). At endpoint, the patients receiving tadalafil reported a greater mean per-patient percentage of successful intercourse attempts (SEP question 3: 70.0%, 10 mg; 78.0%, 20 mg) than placebo-treated patients (42.8%) and a greater proportion of improved erections (GAQ: 92.3% and 84.6% vs. 54.5%). Most treatment-emergent adverse events were mild or moderate. The most common adverse events were back pain, dyspepsia, and myalgia. Conclusions. Tadalafil was an effective, well-tolerated therapy for men in Taiwan with ED of broad-spectrum severity and etiology.
UR - http://www.scopus.com/inward/record.url?scp=20144384249&partnerID=8YFLogxK
U2 - 10.1111/j.1743-6109.2004.04029.x
DO - 10.1111/j.1743-6109.2004.04029.x
M3 - 文章
C2 - 16422975
AN - SCOPUS:20144384249
SN - 1743-6095
VL - 1
SP - 201
EP - 208
JO - Journal of Sexual Medicine
JF - Journal of Sexual Medicine
IS - 2
ER -