Determine the Photoprotection Efficacy of Seven Sunscreen Products Under Visible Light Exposure.

Completed

• Conditions: Visible Light Exposure on Healthy Back Skin

• Registration Number: NCT06796179
• Lead Sponsor: Cosmetique Active International

Brief Summary

To evaluate the protective effect of seven sunscreens on the pigmentation caused by visible light in comparison to an untreated control zone in healthy volunteers.

Detailed Description

The sunscreens usually used as photoprotectors are known to protect in the UV domain (UVB and UVA). However, until recently visible light (400-700 nm) was considered as devoid of any photobiological effects on cutaneous tissue. Over the last two decades, with the development of photodynamic therapies and various dermatological treatments using visible laser light, several studies have reconsidered the cutaneous effect of visible light on the skin, in particular the induction of pigmentation.

The aim of this study was to assess the ability of sunscreens with a protective efficacy in the UV domain to prevent the pigmentation induced by Visible Light.

Study Timeline

• Study Start: 2021-09-03
• Primary Completion: 2021-10-08
• Study Completion: 2021-10-08
• Status Verified: 2025-01
• Study First Submitted: 2025-01-15
• Study First Submitted QC: 2025-01-21
• Last Update Submitted: 2025-01-21
• Study First Posted: 2025-01-28
• Last Update Posted: 2025-01-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Healthy subjects of both sexes aged 18 - 50 years old, having a phototype IIIb, IV or V according to Fitzpatrick classification,
2. Subject with an ITA° (Individual Typologic Angle calculated value) between -20° and 28° at the screening visit,
3. Healthy subjects based on physical examination and compatibility of medical history with the study content,
4. Women of childbearing potential using adequate contraception (oral contraception, intra-uterine devices, contraceptive implants or vaginal rings, tubal sections or ligations, condoms) for at least 1 month prior to first visit and agree to continue adequate contraception during the entire duration of the study,
5. Women of non-childbearing potential (menopausal with one year without bleeding, hysterectomy, bilateral ovariectomy),
6. Subjects having signed a written informed consent form and dated before any study procedure begins.
7. Subjects should be willing to actively cooperate during the study duration and willing to complete the study,
8. Subject affiliated to the social security system (in accordance with the French Law 2004-806 and its implementing decree n°2006-477 of 26 April 2006).

Exclusion Criteria

1. Female who is pregnant or breast feeding or planning a pregnancy during the study,

2. Subject having an underlying known disease, or surgical, physical, or medical condition that, in the opinion of the Investigator might interfere with the interpretation of the clinical trial results such as:

   1. History of recurrent dermatologic conditions (e.g., psoriasis, eczema, urticaria...) or suspicion/history of allergy to cosmetics,
   2. Any systemic or local disease pathology
   3. Skin abnormality (scars, excessive hair, tattoos...) at the level of the test zones (middle part of the back),

3. Subject who has been overexposed to natural (sun) or artificial ultraviolet (tanning lamps) in the last month prior the first visit or who plans a such exposure during the study;

4. Subject having history or presenting pathologies induced or aggravated by sun exposure or having abnormal reactions to the sun (ex : photosensitive dermatitis, polymorphic light eruption, solar urticaria, systemic erythematous lupus, dermatomyositis),

5. Subject having taken a systemic treatment more than 5 days in the month preceding the inclusion (steroids, nonsteroidal anti-inflammatory drugs such as aspirin, antihistamine, insulin, hypertensors, antibiotics such as quinolones, tetracyclins, thiazids, fluoroquinolons and and photosensitizing treatment) or any treatment able to induce abnormal response to UV or visible light (vitamin A derivatives, psoralen, aminolevulinic acid etc.) or having plane to take these treatments during the study,

6. Subjects having applied a local treatment on the back for more than 2 days during the 2 weeks preceding inclusion (steroids, non-steroidal anti-inflammatories, antihistamines, antibiotics) and all other cosmetic products in the previous 24 hours,

7. Subject having antecedents of clinically significant allergy, particularly to study product components,

8. Subjects requiring enhanced protection (deprived of liberty, minors, under guardianship),

9. Subject being in a situation which, according to the Investigator, could interfere with an optimal participation in the study,

10. Subject currently participating or having participated in another clinical trial during the month preceding inclusion,

11. Subject under care of guardian or legal guardianship or subject hospitalized in a medical or social establishment for any reason,

12. Subject unable to communicate efficiently with the Investigator or being unable to follow the study requirements.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Biophysical non-invasive assessment of skin color by using Chromameter® between the exposed zone (ZE) and non-exposed zone (ZNE)	At Day 1 before treatment (baseline), then Day 2, Day 3, Day 4, Day 5 (24 hours after each Visible Light exposure) and Day 12.	Individual Typologic Angle (ITA° - calculated value), •

Secondary Outcome Measures

Name	Time	Method
Clinical investigator's assessment by using clinical scale	At Day 1 before treatment (baseline), then Day 2, Day 3, Day 4, Day 5 (24 hours after each Visible Light exposure) and at Day 12..	Visual scoring of pigmentation, using a pigmentation 11-point scale with 0 (No pigmentation), 1 (Doubtful), 2 (Very pale brown -), 3 (Very pale brown), 4 (Very pale brown +), 5 (Pale brown -), 6 (Pale brown), 7 (Pale brown +), 8 (Brown -), 9 (Brown), 10 (Brown +) Visual scoring of erythema, using an erythema 4-point scale with 0 (Absent), 0.5 (Doubtful), 1 (Weak but well-defined erythema), 2 (Moderate), 3 (Severe)
Safety / Local Tolerance	From the informed consent signature date until the end of the study (Day 12).	Safety was assessed by recording Adverse Events, including cutaneous reactions (local intolerance) assessed using the following 5-point score system: 0 (no sign/symptom of local intolerance); 0.5 (doubtful sign/symptom of local intolerance); 1 (mild sign/symptom of local intolerance); 2 (moderate sign/symptom of local intolerance); 3 (severe sign/symptom of local intolerance)
Biophysical non-invasive assessment of skin color by using Chromameter® between the exposed zone (ZE) and non-exposed zone (ZNE)	At Day 1 before treatment (baseline), then Day 2, Day 3, Day 4, Day 5 (24 hours after each Visible Light exposure) and Day 12.	Erythema (Delta a\* - calculated value)

Trial Locations

Locations (1)

CPCAD (Centre de Pharmacologie Clinique Appliquée à la Dermatologie); 🇫🇷 Nice, France