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

Facial Aging Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01740440
• Other study ID #: SRG-BMR Face01
• Status: Completed
• Phase: Phase 4
• First received: November 21, 2012
• Last updated: November 25, 2013
• Start date: November 2012
• Est. completion date: April 2013

Study information

• Verified date: November 2012
• Source: Bio-Medical Research, Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The primary objective of this clinical study is to evaluate the clinical performance of the BMR Face device (manufactured by Bio-Medical Research) for the overall facial appearance using a grading scale. Secondary objectives are to evaluate safety and further evaluate the subject's and investigator's satisfaction (both a live and blinded assessor) with the BMR Face treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: April 2013
• Est. primary completion date: April 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 35 Years to 55 Years

Eligibility

Inclusion Criteria:

• Subjects who are able to give voluntary, written informed consent to participate in this study and from whom consent has been obtained including HIPAA authorization

• Subjects who are healthy females between 35 and 55 years of age

• Subjects with a Body Mass Index (BMI) between 15-35 kg/m2 (light underweighted to light obese)

• Subjects may have all skin types

• Subjects with age related skin laxity in the treatment area

• Subjects who agree not to have any procedures affecting facial volume (any fillers or fat transfer) for the duration of the study

• Subjects who agree not to have any other procedures affecting skin quality (microdermabrasion, resurfacing, peels, lasers, acne treatments, etc.) for the duration of the study

• Subjects who agree to make no changes in their existing skincare regime during the study period

• Subjects who agree to avoid excessive sun radiation or use appropriate sun protection with SPF 30 or higher

• Subjects who agree not to alter their diet for the duration of the study

• Subjects who understand this study and are able to follow study instructions and are willing to attend the required study visits

• Subjects who agree to be photographed for the purposes of the study and give consent for these photographs to be used in marketing advertisements where their identity will not be concealed in these photographs

Exclusion Criteria:

• Subjects who are pregnant, planning to become pregnant or breastfeeding. A urine pregnancy test will be done to rule out pregnancy.

• Subjects of child-bearing potential who are not using an approved method of birth control (oral contraceptives, IUD, contraceptive implant, barrier methods with spermicide or abstinence)

• Subjects who cannot understand or are not willing to comply with the requirements of the study

• Subjects who have any dermatologic conditions including acne, rosacea, eczema, psoriasis, severe sun damage or scars within the treatment area

• Subjects who have any known cancer including skin cancers (Basal Cell Carcinoma, Squamous Cell Carcinoma and Melanoma)

• Subjects with a history of heart disease or stroke

• Subjects who have any active implanted medical devices (pacemaker, pump etc)

• Subjects having any metal implants. Dental implants and fillings are allowed as well as piercings as long as they are not in the treatment area.

• Subjects who have used a tanning bed in the past four weeks or plan to use a tanning bed for the duration of the study

• Subjects who are HIV positive

• Subjects who have had systemic corticosteroid therapy in the past 6 months

• Subjects who have had a facial dermabrasion, chemical peel, laser, or IPL treatment in the past 6 months

• Subjects who have used botulinum toxin, hyaluronic acid, collagen, fat injections and /or other methods of skin augmentation (enhancement with injected or implanted material) in the past 6 months

• Subjects who have had ablative resurfacing procedure, brow lift, blepharoplasty or face lift in treated area in the past 12 months

• Subjects who have had any other surgery in treated area in the past 12 months

• Subjects who have an existing medical condition that the Investigator considers may put the subject at risk or compromise their participation in the study

• Subjects who have participated in another research study in the past 30 days

• Subjects who are currently involved in any injury litigation claims

• Subjects who have used the BMR Face device previously

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Facial Aging
• Facies

Intervention

Device:
• BMR Face

Locations

Country	Name	City	State
United States	Sadick Research Group	New York	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Bio-Medical Research, Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate the efficacy of the BMR Face device in relation to facial appearance at 12 weeks compared to baseline.	Efficacy will be assessed by overall facial improvement assessed live by the Investigator and a subject assessment of facial appearance including the Global Aesthetic Improvement Scale (GAIS).	12 weeks	No
Secondary	Secondary objectives are to evaluate safety and further evaluate the subject's and investigator's satisfaction (both a live and blinded assessor) with the BMR Face treatment.	Adverse events will be monitored to assess safety.	6 weeks and 12 weeks	Yes
Secondary	Subject satisfaction with the BMR Face Treatment	Subject satisfaction will be measured using subject-completed questionnaire	6 and 12 weeks	No
Secondary	Subject photographs taken to assess outcome of using BMR Face	Subject photographs will be used to assess the overall facial appearance including; Subject photographs will be used to assess overall facial appearance using the Global Aesthetic Improvement Scale	Baseline, 6 and 12 weeks	No
Secondary	Investigator satisfaction of BMR Face Treatment	Investigator's satisfaction with the BMR Face treatment using questionnaire	6 weeks and 12 weeks	No