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A Therapeutic Confirmatory Study to Assess the Safety and Efficacy of Zydena (R) (Udenafil) for the Treatment of Erectile Dysfunction in Male Patients with Diabetes Mellitus

Authors
Moon, Du GeonYang, Dae YulLee, Choong HyunAhn, Tai YoungMin, Kweon SikPark, KwangsungPark, Jong KwanKim, Je Jong
Issue Date
Jul-2011
Publisher
WILEY-BLACKWELL
Keywords
Erectile Dysfunction; Udenafil; Diabetes Mellitus; Pharmacotherapy for Erectile Dysfunction in Men With Diabetes
Citation
JOURNAL OF SEXUAL MEDICINE, v.8, no.7, pp 2048 - 2061
Pages
14
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF SEXUAL MEDICINE
Volume
8
Number
7
Start Page
2048
End Page
2061
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/13335
DOI
10.1111/j.1743-6109.2011.02268.x
ISSN
1743-6095
1743-6109
Abstract
Introduction. Patients with diabetes mellitus (DM) are reported to experience more severe erectile dysfunction (ED) symptoms and respond less to ED treatments compared with patients with ED of other etiologies. Aim. This study was undertaken to evaluate the safety and efficacy of udenafil for the treatment of ED in a larger number of patients with DM. Methods. A placebo-controlled, randomized, double-blind, double-dummy, parallel-group design multicenter study, fixed-dose trial was conducted. The trial involved seven study sites in Korea, with 174 ED patients with DM. The subjects, treated with placebo, 100 mg, or 200 mg of udenafil for 12 weeks, were asked to complete the International Index of Erectile Function (IIEF), the Sexual Encounter Profile (SEP) diary, and the Global Assessment Question (GAQ) during the study period. Main Outcome Measures. The primary efficacy parameter was the change in the erectile function domain (EFD) score of IIEF from baseline. Secondary parameters were IIEF questions 3 (Q3) and Q4, SEP Q2 and Q3, rate of achieving normal erectile function (EFD >= 26), and the response to GAQ. Results. Compared with the placebo, patients receiving both doses of udenafil showed statistically significant improvements in the IIEF-EFD score, respectively. However, statistically significant difference was not observed between the udenafil 100 mg and the udenafil 200 mg groups. Similar results were observed in the comparison of Q3 and Q4 of IIEF, SEP diary, and GAQ. The percentages of subjects experiencing at least one adverse event related to the study drugs were 3.6%, 15.8%, and 22.4% for the placebo, udenafil 100 mg, and udenafil 200 mg groups, respectively. However, these events were all mild in severity. Major adverse events were flushing, headache, nausea, and conjunctival hyperemia. Conclusion. Udenafil was significantly effective for the treatment of ED, demonstrating statistically significant improvement in erectile function in patients with DM. The incidence of adverse events was relatively low and well tolerated in patients with DM. Moon DG, Yang DY, Lee CH, Ahn TY, Min KS, Park K, Park CK, and Kim JJ. A therapeutic confirmatory study to assess the safety and efficacy of Zydena (R) (udenafil) for the treatment of erectile dysfunction in male patients with diabetes mellitus. J Sex Med 2011;8:2048-2061.
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