drugset / Trial / NCT01423370
Safety and Efficacy of YHD1023 in Erectile Dysfunction
RandomizedParallel-groupDouble-blindTreatment
Summary
The objective of this study is to assess the safety and efficacy of oral YHD1023 5g or 10g on erectile dysfunction to investigate the optimal recommended dosage. Study period is 12 weeks including 4weeks of follow-up period without treatment. Study patients will fill in the international index of erectile function questionnaire and life satisfaction questionnaires.
Timeline
- Start
- 2011-11
- Primary completion
- 2013-03
- Completion
- 2013-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Tadalafil | Small molecule | 5 mg | Oral |
| Subject | YHD1023 | Unknown | 5 g | Oral |
| Subject | YHD1023 | Unknown | 10 g | Oral |