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

Medytox

Status: Completed

Conditions: Penile Girth Enhancement; Penile Enhancement

Treatments: Device: Potenfill

Study type: Interventional

Funder types: Industry

Identifiers

NCT03840070

MT05-KR18PGE1005

Details and patient eligibility

About

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.

Enrollment: 20 patients

Sex: Male

Ages: 19 to 65 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Potenfill

Experimental group

Treatment:

Device: Potenfill