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The Efficacy of the Me Mini Device for Hair Removal

NCT02912013 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2018-03-09

No results posted yet for this study

Summary

The Mē Mini is a compact version of the Mē device that was cleared by the FDA for removal of unwanted hair and for permanent hair reduction for all skin colors (Fitzpatrick skin photo-types I-VI) based on a series of multi-site clinical studies.

The purpose of this post-marketing study is to support the claims for removal of unwanted hair and for permanent hair reduction in the compact version of the device.

Conditions

  • Hair Removal

Interventions

DEVICE

Me Mini

Home use hair removal device

Sponsors & Collaborators

  • Iluminage Ltd.

    lead INDUSTRY

Principal Investigators

  • David J Friedman, MD · Friedman Laser & Skin Center

  • Lilach Gavish, PhD · HUJI

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2017-11-03
Completion
2018-03-01

Countries

  • Israel

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 NCT02912013 on ClinicalTrials.gov