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Evaluate the Efficacy and Safety of MINTLIFT® Group for Nasolabial Fold

NCT01848717 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2013-05-07

No results posted yet for this study

Summary

The objective of this clinical test is to verify the safety and efficacy of MINTLIFT®, used for the purpose of improving the appearance of the nasolabial fold on both sides of the face.

Conditions

  • Nasolabial Fold

Interventions

DEVICE

MINTLIFT®

Sponsors & Collaborators

  • HansBiomed Co.,Ltd.

    collaborator INDUSTRY

  • Chung-Ang University Hosptial, Chung-Ang University College of Medicine

    lead OTHER

Principal Investigators

  • Beom Joon KIM, MD, PhD · Department of Dermatology

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-12-31

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 NCT01848717 on ClinicalTrials.gov