Virginia Beach, Virginia 23462

  • Blue Light Damage

Purpose:

To evaluate 10 days of pretreatment with a serum (Test Product/Marvel AM) to the lower back, followed by a single exposure of 90J/cm2 HEV (High Energy Visible) light {400-450nm wavelengths} in healthy male or female volunteers.


Criteria:

Inclusion Criteria: - Volunteers can be male or female, 18 to 65 years of age with no known medical conditions that, in the investigator's opinion, may interfere with study participation. - Volunteers must sign a written informed consent. - Volunteers must fall within Fitzpatrick Skin Type I-V. - Volunteers must be willing to avoid sun exposure to the study treatment area (lower back) for the duration of the study. - Volunteers must commit to meeting all study requirements, including 11 days of sequential office visits for product application, HEV exposure, biopsy and suture removal. Exclusion Criteria: - Volunteers who are pregnant, breast feeding or planning a pregnancy during the study period. - Have used within the month before inclusion, any systemic medication for more than 5 consecutive days (e.g. steroidal and non-steroidal anti-inflammatory drugs, insulin, antihistamines, antihypertensive, antibiotics-e.g quinolone, tetracycline, thiazides, fluoroquinolones), or any medication known to cause abnormal responses to HEV light exposure (e.g. vitamin A derivatives, psoralen, aminolevulinic acid derivatives, etc.), or having planned to use these medications during the study. - Volunteers who have damaged skin in close proximity to test sites (e.g. sunburn, uneven skin tones, tattoos, scars or other disfigurations) - Volunteers who have used a prescription hydroquinone, non-hydroquinone skin lightening or brightening agent, or like product in the test area, within the past 3 months. - Volunteers who have used a non-prescription cosmetic anti-aging or skin lightening product known to affect dyschromia or hyperpigmentation, in the test area, within the past 4 weeks. - Volunteers who have a history of scarring, hypertrophic scarring or keloid formation anywhere on their body. - Volunteers with a known sensitivity to lidocaine or epinephrine. - Volunteers who are unwilling or unable to comply with the requirements of the protocol, including ability to complete all study visits within the proscribed study visit window for any reason(s). - Volunteers with any disorder that may prevent compliance, such as history of chronic alcohol or drug abuse, significant mental or nervous disorder or other illness that would, in the evaluator's opinion, interfere with the study. - Have participated, or are participating in, another study within the past 4 weeks. - Any dermatologic disorder which, in the investigator's opinion, may interfere with the accurate evaluation of the study treatment area (lower back), but not limited to melasma, any active inflammatory skin condition (i.e. post inflammatory hyperpigmentation), severe acne vulgaris, acne conglobata, acne fulminans, seborrheic dermatitis, and lupus erythematosus. - Volunteers who have demonstrated a previous hypersensitivity reaction to any of the ingredients of the study products. - Concurrent therapy with any medication either topical or oral which, in the investigator's opinion, may interfere with evaluation.


NCT ID:

NCT03594721


Primary Contact:

Study Director
Elizabeth Makino
Allergan


Backup Contact:

N/A


Location Contact:

Virginia Beach, Virginia 23462
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 22, 2021

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.