Clinical Trials Directory

Trials / Completed

CompletedNCT06616558

A Study to Assess the Effectiveness of Sunscreen on Oil Control, Moisturization, and Skin Barrier Integrity in Adults With Oily Skin

A Single-Center, Open-Label, Randomized Clinical Study to Evaluate the Oil Control Efficacy, Moisture Assessment and Skin Barrier Integrity of an Investigational Product in Adult Participants With Oily Facial Skin

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
JNTL Consumer Health (Brasil) LTDA · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The purpose of this trial is to evaluate 1) the efficacy of an investigational product (sunscreen) when compared to a control area (without product application) in controlling oiliness, oil shine and the effect on pores appearance in a 12-hour kinetics through a) Instrumental measurements, b) Expert Grader and c) Perceived efficacy; 2) the efficacy of an investigational product in reducing oiliness, improving hydration, the pores appearance and the integrity of the skin barrier, after 7 days of use and after 28 ± 2 days of use through instrumental measurements and perceived efficacy questionnaires.

Detailed description

The objectives of this study are: To evaluate the efficacy of an investigational product (sunscreen) when compared to a control area (without product application) in controlling oiliness, oil shine and the effect on pores appearance in a 12-hour kinetics: * Instrumental measurements with the Sebumeter® SM 815 equipment to assess oiliness control; * Clinical efficacy evaluation carried out by Expert Grader * Perceived efficacy through perception questionnaires To evaluate the efficacy of an investigational product in reducing oiliness, improving hydration, pores appearance and the integrity of the skin barrier, after 7 days of use and after 28 ± 2 days of use, under normal conditions of use in adult participants through the following evaluations: * Instrumental measurements with the Sebumeter® SM 815 equipment before and after 7 and 28 ± 2 days of use on the face to assess oil reduction; * Instrumental measurements with the Corneometer® before and after 7 and 28 ± 2 days of use on the face to assess skin hydration; * Instrumental measurements with the Tewameter® TM 300 before and after 7 and 28 ± 2 days of use on the face to assess the integrity/maintenance of the skin barrier; * Facial images captured using Visia® CR equipment before and after 7 and 28 ± 2 days of use on the face; * Perceived efficacy through perception questionnaires answered by research participants after 7 and 28 ± 2 days of use on the face; * Open-ended emotional statement after 28 ± 2 days.

Conditions

Interventions

TypeNameDescription
OTHERSunscreen SPF 70Participants will topically apply sunscreen SPF 70
OTHERSunscreen SPF 70On the randomized side of the half-face, the product will be applied by a qualified technician

Timeline

Start date
2024-06-03
Primary completion
2024-07-30
Completion
2024-07-30
First posted
2024-09-27
Last updated
2024-09-27

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT06616558. Inclusion in this directory is not an endorsement.