Last updated: 11/30/2021 05:50:03
Clinical Study to Evaluate the Sun Protection Factor (SPF) of Sunscreen Products
GSK study ID
218003
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Clinical Evaluation of the Sun Protection Factor (SPF) of Sunscreen Products According to the FDA Final Rule: Sunscreen Drug Products (2011)
Trial description: The purpose of this study is to determine the static SPF of three sunscreen products (ChapStick Lip Moisturizer [CLM] Original, CLM Mint Flavour and CLM Black Cherry Flavour) using the methodology described in the Food and Drug Administration (FDA) Final Rule (2011).
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
Single (Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:
Arithmetic Mean of Individual Sun Protection Factor (SPFi) Values
Timeframe: Up to 24 hours post UV exposure
Secondary outcomes:
Not applicable
Interventions:
Enrollment:
11
Primary completion date:
2021-04-11
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Sunscreening Agents
Product
Not applicable
Collaborators
Not applicable
Study date(s)
October 2021 to November 2021
Type
Interventional
Phase
Not applicable
Participation criteria
Sex
Female & Male
Age
18 - 70 Years
Accepts healthy volunteers
Yes
- Participant must provide a signed and dated, legally effective, informed consent document, which indicates they have been informed of all pertinent aspects of the study, before any study procedures are performed.
- Participant must provide relevant details of their medical history and current/recent medications and treatments (self-reported).
- Participant with a scheduled or planned Covid-19 vaccination during likely dates of study participation.
- Participant with a history of abnormal response to sunlight/UV radiation.
Inclusion and exclusion criteria
Inclusion criteria:
- Participant must provide a signed and dated, legally effective, informed consent document, which indicates they have been informed of all pertinent aspects of the study, before any study procedures are performed.
- Participant must provide relevant details of their medical history and current/recent medications and treatments (self-reported).
- Participant must have completed an annual Health Insurance Portability and Accountability Act (HIPAA) Authorization form.
- Participant must have completed a Photo Release Form.
- Participant must be able to read, write, speak and understand English.
- Participant must be in good general health.
- Participant must have uniform skin color over the test area (skin of the back between the shoulder blades and above the waistline) and an Individual Typology Angle (ITA) value more than (>)28 degree.
- Participant must have Fitzpatrick Skin Type I, II or III
- Participant must have sufficient area of suitable skin on their back for at least six 40 centimeter square (cm^2) test sites.
- Willing to have body hair clipped by a technician if participant has excessive hair in the test area.
- Participant must have a valid form of personal identification (photo identity [ID], driver’s license, passport, permanent resident card, military ID card; forms cannot be expired).
- Male and female participants of child-bearing potential must agree to use a highly effective method of contraception for the duration of the study and for 14 days after their last treatment application. (Note: Note: A participant is considered to be of child-bearing potential if, in the opinion of the Principle Investigator (PI), they are biologically capable of having children and sexually active.
Exclusion criteria:
- Participant with a scheduled or planned Covid-19 vaccination during likely dates of study participation.
- Participant with a history of abnormal response to sunlight/UV radiation.
- Participant with a history of sensitivity to any ingredient of the test material or skin marker pen, or to latex; or any known sensitivities/allergies, including but not limited to cosmetic/toiletry products and topically applied skin treatment products/drugs.
- Participant with any significant dermatological condition, such as atopic dermatitis (eczema), psoriasis, skin cancer, melanoma, active dermal lesions, nevi, blemishes or moles, lupus, diabetes, or connective tissue disease, that would increase the risk associated with participation. (Note: presence of non-dysplastic nevi, blemishes, or moles would be acceptable if, in the opinion of the PI, they will neither jeopardize participant safety or compromise study outcomes. A participant with dysplastic nevi should be disqualified.
- Participant receiving any treatment with medications that would, in the opinion of the PI, confound study outcomes or increase the risk associated with participation, such as systemic or topical corticosteroids, antibiotics, anti-inflammatory drugs, antihistamines, antihypertension medications, or any other photosensitive medications. (Note: The prohibited medication list will be available to site staff for reference during screening)
- Participant who has used topical or systemic steroids, antihistamines, antibiotics or anti-inflammatory medications within 7 days of Study Day 1 which, in the opinion of the PI, could interfere with study outcomes.
- Participant who has used/applied any personal care products (for example, lotions, sunscreens, sunless tanners) and/or topical medications in/on the test area within 24 hours of Study Day 1.
- Participant who is unwilling to cease use of personal care products (for example, lotions, sunscreens, sunless tanners) and/or topical medications in/on the test area for the duration of the study.
- Participant with any known communicable disease(s) (for example, Human Immunodeficiency Virus [HIV], Sexually Transmitted Diseases [STD’s], Hepatitis B, Hepatitis C, and so on)
- Participant with skeletal protrusions and/or extreme areas of curvature in the test area.
- Participant with a medical treatment/vaccination (other than the Covid-19 vaccination) planned during the study, which would make them ineligible, place them at undue risk, or confound the outcome of the study, per the discretion of the PI.
- Participant who has undergone any surgical procedure in the last 12 months.
- Participant who has undergone chemical or physical treatment procedures in the test area within the last 12 months.
- Planned hospitalization during the study.
- Participant who exceeds a weight limit of 300 pounds due to equipment limitations.
- Participant with any condition that might confound the study results, increase the risk associated with participation, or interfere with study participation.
- Female participant who is pregnant, planning to become pregnant during the study, or breastfeeding (self-reported).
- Participant with any visible sunburn or suntan in test area.
- Participant with visible sun damage, scarring or tattoos in the test area that would interfere with study participation.
- Participant with any sun exposure and/or use of an artificial tanning lamp on the test area within 2 months of Study Day 1.
- Participant who is unwilling to avoid sun exposure and/or cease use of an artificial tanning lamp on the test area for the duration of the study.
- Participant who has participated in any clinical study involving UV exposure within the last 2 months, or any other type of clinical study within the last 1 month.
- Participant who is an employee/contractor or immediate family member of the PI, study site or Sponsor.
Trial location(s)
Location
GSK Investigational Site
Winston-Salem, North Carolina, United States, 27101
Status
Study Complete
Study documents
No study documents available.
Results overview
Study Results yet to be posted
Recruitment status
Study complete
Actual primary completion date
2021-04-11
Actual study completion date
2021-04-11
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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