MedPath

A randomized, double blinded, split-face clinical study of the efficacy of using Eucerin Sun Dry Touch Sebum Control DP to reduce post inflammatory hyperpigmentation after Picosecond laser

Phase 4
Conditions
mild to moderate acne vulgaris with mild to moderate acne scars
Eucerin Sun Dry Touch Sebum Control DP, Post inflammatory hyperpigmentation, Picosecond laser, Sunscreen, Acne vulgaris
Registration Number
TCTR20210305004
Lead Sponsor
Beiersdorf Thailand
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
All
Target Recruitment
60
Inclusion Criteria

1. male/female at least 18 years of age
2. mild-moderate acne vulgaris with mild-moderate acne scars
3. Fitz patrick skin phototype 3 or 4
4. able to comply with study protocol
5. willingly inform consent

Exclusion Criteria

1. unable to stop previous treatment (washout period; systemic treatment for acne 3 months, laser/phototherapy 1 month, topical treatment is 2 weeks).
2. having infection or other facial dermatologic conditions at treatment site.
3. Polycystic Ovary Syndrome (PCOS)
4. Pregnant or lactating women
5. allergic to study product.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post inflammatory hyperpigmentation Wk 0 ,1, 2, 4, 6 Visia (Brown spots)
Secondary Outcome Measures
NameTimeMethod
Acne count Wk 0 ,1, 2, 4, 6 Acne count,Porphyrin Wk 0 ,1, 2, 4, 6 Visia (Porphyrin),Patient satisfaction score Wk 1, 2, 4, 6 Patient satisfaction score (0-10),Acne scars Wk 1, 2, 4, 6 quartile grading scale (evaluated by dermatologist)
© Copyright 2025. All Rights Reserved by MedPath