A Clinical Trial to Evaluate the Effectiveness of an Acne Serum in Improving Facial Acne and Post-Acne Pigmentation
- Conditions
- Acne
- Registration Number
- NCT06120452
- Lead Sponsor
- Rael
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria:<br><br> - Female. Age 18+. Currently experiencing mild to moderate acne issues. Generally<br> healthy -and not living with any uncontrolled chronic disease.<br><br>Exclusion Criteria:<br><br> - Anyone with pre-existing chronic conditions that would prevent participants from<br> adhering to the protocol, including oncological and psychiatric disorders.<br><br>Anyone currently using an oral and/or topical prescription acne treatment. Anyone<br>unwilling to stop using their current acne supplements. Anyone with known severe allergic<br>reactions. Anyone unwilling to avoid excessive sun exposure. Anyone who is breastfeeding,<br>pregnant, or attempting to become pregnant. Anyone unwilling to follow the study<br>protocol. Anyone who identifies as having sensitive skin.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in the appearance of facial acne. [Timeframe: Baseline to Day 56];Changes in the appearance of post-acne pigmentation. [Timeframe: Baseline to Day 56]
- Secondary Outcome Measures
Name Time Method Changes in facial skin hydration. [Timeframe: Baseline to Day 56];Changes in facial skin softness. [Timeframe: Baseline to Day 56];Changes in facial skin texture. [Timeframe: Baseline to Day 56]