NCT03303170
Completed
N/A
A Prospective, Multicenter, Randomized, Controlled, Evaluator-Blinded Study of the Safety and Effectiveness of Sebacia Microparticles as an Accessory to 1064 nm Nd:Yag Laser in the Treatment of Facial Inflammatory Acne Vulgaris
Sebacia, Inc.11 sites in 1 country168 target enrollmentSeptember 25, 2017
ConditionsAcne Vulgaris
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Acne Vulgaris
- Sponsor
- Sebacia, Inc.
- Enrollment
- 168
- Locations
- 11
- Primary Endpoint
- Change in number of inflammatory acne lesions
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
Prospective, randomized, controlled, parallel group clinical study with blinded assessment evaluating Sebacia Microparticles (SM) with Nd:Yag laser in facial inflammatory acne vulgaris
Investigators
Eligibility Criteria
Inclusion Criteria
- •Mild to moderate acne vulgaris
- •At least 15 inflammatory acne lesions
- •Skin phototype I - III
- •Able to understand and comply with study requirements
Exclusion Criteria
- •Severe acne vulgaris
- •Nodulocystic acne
- •Ongoing use of medications and/or treatments for acne
- •New hormone regimen (used for less than 12 weeks)
- •Significant medical or mental health condition
Outcomes
Primary Outcomes
Change in number of inflammatory acne lesions
Time Frame: Week 12
Study Sites (11)
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