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A Multi-center, Randomized, Subject Blind, Active Controlled Design Clinical Study to Evaluate the Efficacy and Safety of Volus as Compared to PowerFill® for Temporary Penile Enhancement

NCT02833532 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2017-08-08

No results posted yet for this study

Summary

The purpose of this study is to evaluate non-inferial study of the after using Volus application, compared to the powerfill.

Conditions

  • Penile Enhancement

Interventions

DEVICE

Volus/Powerfill

Maximum: 22ml

Sponsors & Collaborators

  • Associacio catalana per a la recerca oncologica i les seves implicacions sanitaries i socials

    collaborator OTHER

  • Hugel

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-01-31
Completion
2017-06-30

Countries

  • South Korea

Study Locations

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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 NCT02833532 on ClinicalTrials.gov