Efficacy and Safety of Potenfill for Temporary Penile Enhancement

NCT03512717 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2019-03-26

No results posted yet for this study

Summary

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

Conditions

  • Penile Enhancement

Interventions

DEVICE

Potenfill

Maximum: 22ml

DEVICE

Powerfill

Maximum: 22ml

Sponsors & Collaborators

  • Medy-Tox

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
65 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-11-16
Primary Completion
2018-07-31
Completion
2018-07-31

Countries

  • South Korea

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03512717 on ClinicalTrials.gov