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Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance

NCT01740440 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-06-30

Study results available
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Summary

Safety and clinical performance of the BMR Face device (manufactured by Bio-Medical Research)

Conditions

  • Ageing

Interventions

DEVICE

BMR Face

BMR Face used in accordance with manufacturer IFU

Sponsors & Collaborators

  • Bio-Medical Research, Ltd.

    lead INDUSTRY

Principal Investigators

  • Neil Sadick, Dr · Sadick Research Group

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
35 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • United States

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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 NCT01740440 on ClinicalTrials.gov