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
| Type | Name | Description |
|---|---|---|
| OTHER | Sunscreen SPF 70 | Participants will topically apply sunscreen SPF 70 |
| OTHER | Sunscreen SPF 70 | On 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.