The Efficacy and Safety of Repeat-dose Potenfill for Temporary Penile Enhancement

Medy-Tox20 enrolled

Overview

This clinical study is for small-penis syndrome males who have previously been treated with hyaluronic acid filler for the purpose of increasing their penis. This study will determine the long-term efficacy and safety of Potenfill.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Penile Girth Enhancement Penile Enhancement

Interventions

PotenfillDEVICE

Maximum: 22ml

Eligibility

Sex: MALEMin age: 19 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Male subjects aged above 19 and below 65. (20≤male≥65) * Subjects will sign an informed consent form Exclusion Criteria: * Prior treatment for penile enhancement (e.g. fat, dermal graft). * Allergic to hyalluronic acid.

Locations (1)

Korea university guro hospital

Seoul, South Korea

Outcomes

Primary Outcomes

Subject satisfaction on the penile appearance at 12 months after application of Potenfill

Satisfaction with the physical appearance of penis as assessed by the subject at 12 months after the application of investigational medical device.

Time frame: 12 month

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.