Study on safety and efficacy of Lipen-D on glans penis augmentatio
Not Applicable
Completed
- Conditions
- Diseases of The genitoruinary system
- Registration Number
- KCT0002066
- Lead Sponsor
- Chunghwa Medipower
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Male
- Target Recruitment
- 20
Inclusion Criteria
healthy men, aged 20 or over
- men with small penis syndrome
- during the study period, subject will not received any treatments associated with penile augmentation
- subject will agree with investigator's decision
- subject will sign an informed consent form
Exclusion Criteria
- any history of psychological or psychiatric illness,
- congenital or acquired penile malformation including severe phimosis,
- previous penile augmentation history,
- any chronic major systemic disease including diabetes and coagulopathy
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method an increase in glans surface area of 20% or more.
- Secondary Outcome Measures
Name Time Method subject satisfaction