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MĒ Device for At-Home Skin Rejuvenation

NCT02902718 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2017-03-03

No results posted yet for this study

Summary

The purpose of this pilot study is to evaluate the feasibility of the Mē device for at home facial skin rejuvenation.

Conditions

  • Skin Aging
  • Skin Rejuvenation

Interventions

DEVICE

mē

The mē device will be used for self administered facial treatments that will be repeated up to 3 times every session. The duration of a treatment session is 5-10 minutes.

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
25 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-28
Primary Completion
2017-09-30
Completion
2017-12-31
FDA Device
Yes

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 NCT02902718 on ClinicalTrials.gov