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The Efficiency of the Hair2Go Device: A Prospective, Open, Label Study With Before-After Design

NCT01348776 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 87

Last updated 2013-04-04

Study results available
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Summary

The purpose of this study is to determine efficiency of Hair2Go device for short-term and long-term removal of unwanted hair adjunctive to shaving using a before-after study design.

Conditions

  • Hair Removal

Interventions

DEVICE

Hair2Go (Mē)

Treatment with Hair2Go Device 7 times every week with maintenance treatments once a month for 3 months

Sponsors & Collaborators

  • Syneron Medical

    lead INDUSTRY

Principal Investigators

  • Jerome M Garden, MD · Northwestern Memorial Hospital

  • Vince Afsahi, MD · South Coast Dermatology Institute

  • Brian D Zelickson, MD · Abbot Northwestern Hospital Center for Cosmetic Care

  • Michael Gold, MD · Tennessee Clinical Research Center

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
2011-03-31
Primary Completion
2012-06-30
Completion
2012-06-30

Countries

  • United States

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 NCT01348776 on ClinicalTrials.gov