Evaluation of Sunscreens Under Actual Use Conditions

NCT ID: NCT02952235

Last Updated: 2017-06-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 199 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-03-31
• Study Completion Date: 2016-03-31

Brief Summary

Use of two high SPF sunscreens under actual use conditions.

Detailed Description

To evaluate the difference in the level of sunburn (erythema) protection following a single period of natural sunlight exposure afforded by application of SPF 50+ and SPF 100+ sunscreens.

Conditions

Sun Protection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: TRIPLE

Study Groups

SPF50+

SPF 50+ assigned to Left side of face SPF 100+ assigned to Right side of face

Group Type: OTHER

SPF50+

Intervention Type: OTHER

Sun protection

SPF100+

SPF 100+ assigned to Left side of face SPF 50+ assigned to Right side of face

Group Type: OTHER

SPF100+

Intervention Type: OTHER

Sun protection

Interventions

SPF50+

Sun protection

Intervention Type: OTHER

SPF100+

Sun protection

Intervention Type: OTHER

Other Intervention Names

Sunscreens; Sunscreens

Eligibility Criteria

Inclusion Criteria

1. Males and Females with Fitzpatrick Skin Types I-III

2. At least 18 years old

3. Able to read, write, speak and understand the English language.

4. Has personally read, signed, and dated the Informed Consent Form (including HIPAA disclosure) and Photograph Release

5. Generally in good health based on medical history reported by the subject

6. Healthy male or female subjects with no history or evidence of clinically relevant medical disorder, as determined from a brief medical history interview.

7. Willing and able to follow the study instructions, including:

Remain outdoors for at least 5 hours on Day 1 during the study with face and neck uncovered (as much as possible)

• Apply the test products (sunscreen) to designated sides of the face and neck
• Remove any make-up, sunscreen, or other facial products at baseline prior to applying test product. Use test product in place of current sun protection topical skincare products (this includes make-up)
• Attend scheduled visits and intend to successfully complete the study
• Return ALL study products at Day 2 exit visit
• Refrain from using other sunscreen products or tanning bed use during the duration of the study.

Exclusion Criteria

1. Individuals with known allergies or sensitivities to sunscreens or any ingredient contained in the test products or common topical skincare products, including adhesives.

2. Observable Sunburn (erythema score above 0.5) on the face and neck as determined by the PI or designee.

3. Women known to be pregnant or nursing.

4. Individuals with any disease or condition of the skin (e.g., active [i.e. flaring] eczema or psoriasis, skin cancer, polymorphic light eruption (PMLE), systemic lupus erythematous (SLE), xerodermapigmentosa) that could interfere with the study or increase risk to the subject.

5. Individuals with self-reported UNCONTROLLED metabolic conditions, such as diabetes, hypertension, hyper/hypothyroidism, hypercholesterolemia

6. Subjects who are taking medication for chronic conditions that may make a subject more sun sensitive (e.g., Tetracyclines, antifungals, certain diuretics, etc.)

7. Skin diseases on tested sites (e.g., photosensitivity disorders, etc.), which may influence the outcome of the study

8. Wearing of a full head covered ski mask.

9. An individual who has any condition which in the PI's judgment makes the candidate an inappropriate subject for study participation

10. Subjects who are related to those persons involved directly or indirectly with the conduct of this study (i.e., PI, sub-investigators, study coordinators, other site personnel, employees of Johnson & Johnson subsidiaries, contractors of Johnson & Johnson, and the families of each)

11. Individuals with a condition or situation which, in the PI's opinion, may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study

12. Individual viewed by the PI as not being able to complete the study

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Johnson & Johnson Consumer and Personal Products Worldwide

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Joshua Williams, PhD

Role: STUDY_DIRECTOR

Sponsor GmbH

Other Identifiers

CO-151112132858-SACT

Identifier Type: -

Identifier Source: org_study_id