Efficacy and Safety of Potenfill for Temporary Penile Enhancement

Medytox

Status: Completed

Conditions: Penile Enhancement

Treatments: Device: Potenfill; Device: Powerfill

Study type: Interventional

Funder types: Industry

Identifiers

NCT03512717

MT05-KR17PGE308

Details and patient eligibility

About

The purpose of this study is to evlauate the efficacy and safety of poteinfill, compared to the powerfill.

Enrollment: 76 patients

Sex: Male

Ages: 19 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Male subjects aged above 19 and below 65. (20≤male≥65)
2. be rating himself, when screening, as "Small or Very Small" on Self-Questioned Questionnaire ( SQQ) including the question: " How do you rate your penile size? // Very small, Small, Normal, Big, Very Big?"
3. Subjects will sign an informed consent form

Exclusion criteria

1. Prior treatment for penile enhancement (e.g. fat, dermal graft).
2. Subjects who have penile malformation (e.g. Peyronie's disease), which can make impossible to perform the intervention
3. Allergic to hyalluronic acid.
4. Inflammatory or/and infectious disease on penis that can affect on this study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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76 participants in 2 patient groups

Potenfill

Experimental group

Treatment:

Device: Potenfill

Powerfill

Active Comparator group

Treatment:

Device: Powerfill