An Exploratory Study to Evaluate Skin Brightening Effects of Different Cosmetic Formulations on UV Irradiated Tanning Model

NCT07795866 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 13

Last updated 2026-08-31

No results posted yet for this study

Summary

This is a double-blind randomized, complete block design study on Chinese population, expecting approximately 18 participants recruited and at least 10 participants to complete the whole 9-week study. The study test sites will receive a single 2MED UV radiation .

Conditions

  • Skin Brightening

Interventions

OTHER

SMR 1

Cosmetic skin brightening product to be applied to defined test site

OTHER

SMR 2

Cosmetic skin brightening product to be applied to defined test site

OTHER

SMR 3

Cosmetic skin brightening product to be applied to defined test site

OTHER

SMR 4

Cosmetic skin brightening product to be applied to defined test site

OTHER

SMR 5

Cosmetic skin brightening product to be applied to defined test site

OTHER

Pro-Derma 1

Cosmetic skin brightening product to be applied to defined test site

OTHER

Pro-Derma 2

Cosmetic skin brightening product to be applied to defined test site

OTHER

Pro-Derma 3

Cosmetic skin brightening product to be applied to defined test site

OTHER

Pro-Derma 4

Cosmetic skin brightening product to be applied to defined test site

OTHER

Pro-Derma 5

Cosmetic skin brightening product to be applied to defined test site

OTHER

Thiamidol

Cosmetic skin brightening product to be applied to defined test site

Sponsors & Collaborators

  • Unilever R&D

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-09-10
Primary Completion
2026-11-11
Completion
2026-11-11

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07795866 on ClinicalTrials.gov