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Evaluation of the Efficacy and Tolerance of a Light Therapy Mask on Mild to Moderate Brown Spots and Moderate to Severe Facial Wrinkles

Johnson & Johnson (J&J) logo

Johnson & Johnson (J&J)

Status

Completed

Conditions

Skin Aging

Treatments

Device: Sham Mask
Device: Active Mask

Study type

Interventional

Funder types

Industry

Identifiers

NCT03312543
CO-170511132943-SACT

Details and patient eligibility

About

This research study will test how well a light therapy mask works for women with mild to moderate hyperpigmentation (brown spots) and moderate to severe facial wrinkles, as compared to a "sham" or inactive investigational light therapy mask. The study will also test if the light therapy mask causes any irritation. For the first 12 weeks of the study, participants will use the assigned mask, along with a provided cleanser and sunscreen. For the second 12 weeks of the study, participants will use just the cleanser and sunscreen.

Full description

Exposure to sunlight and artificial light sources containing ultraviolet (UV) radiation is known to accelerate the skin's aging process, resulting in unwanted wrinkles, irregular skin tone, and loss of elasticity. Ablative techniques, such as dermabrasion, deep chemical peels, and ablative laser resurfacing of various wavelengths, are well documented to alleviate the signs of photodamage. However, such techniques often require significant post-treatment care and have higher risk profiles than other treatments, with potential side effects including erythema, pigmentation issues, infection, and possible scarring. They may be poorly tolerated by patients who dislike the discomfort, wound care, and prolonged downtime involved.

Non-ablative skin rejuvenation procedures are also effective for improving the appearance of photodamaged skin and are becoming increasingly popular because of their minimal downtime and increased safety. These procedures include intense pulsed light systems, non-ablative lasers, and monochromatic light boxes, which can target facial rhytids, irregular pigmentation, telangiectasia, and skin laxity. Unfortunately, such techniques can be expensive and their use is primarily limited to clinical settings.

However, the light-emitting diode (LED) is a novel light source that is well-suited for non-ablative phototherapy that can be utilized at home for a relatively low price. This study will evaluate the efficacy and tolerance of an LED-based light therapy mask as compared to a sham mask in subjects seeking anti-aging benefits.

Enrollment

124 patients

Sex

Female

Ages

35 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Has mild to moderate brown spots
  • Has moderate to severe facial wrinkling
  • Able to read, write, speak, and understand English
  • In general good health
  • If capable of having a child: must agree to practice a medically acceptable form of birth control.
  • Intends to complete the study and willing to follow all study directions.

Exclusion criteria

  • Allergies/sensitivity to skincare products or the test product ingredients
  • Has a light or photosensitivity disorder or another medical condition that could increase risk to the subject or confuse the study results.
  • Is taking medication that may cause skin sensitivity to light
  • Has been using a product or medication that the study investigator determines will increase health risk to the subject or confuse the study results
  • Has a facial skin condition (e.g. rosacea, acne, eczema, etc.) that could increase health risk to the subject or confuse the study results.
  • Has skin cancer or a history of skin cancer.
  • Has an immune deficiency disorder, active hepatitis, or an autoimmune disease.
  • Has an uncontrolled metabolic condition (e.g. diabetes, hypertension)
  • Is pregnant, nursing, or planning to become pregnant.
  • Plans to start or change a hormone replacement therapy during the study.
  • Has participated in another study in the past 30 days or plans to during the study.
  • Is an employee or relative of the Study Site, Investigator, or Sponsor.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

124 participants in 2 patient groups

Active Cell: Active Mask
Experimental group
Description:
Cleanser, Moisturizer, Active Mask
Treatment:
Device: Active Mask
Sham Cell: Sham Mask
Sham Comparator group
Description:
Cleanser, Moisturizer, Sham Mask
Treatment:
Device: Sham Mask

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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