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An analysis of the factors involved in acne vulgaris

Not Applicable
Conditions
Acne vulgaris
Registration Number
JPRN-UMIN000019445
Lead Sponsor
Kao Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

1_Individuals who contract diabetes, HIV/AIDS or autoimmune disorders, and hepatitis B or C. 2_Individuals with cuts, lacerations, abrasions, or bruises on the biopsy sites 3_Individuals with tattoos on the biopsy sites. 4_Individuals who participated in other clinical study within 28days. 5_Individuals with allergies (self-reported) to wound dressings and adhesives, latex allergy or allergies towards the local anesthetic. 6_Individuals with any relevant past or present medical history which may affect the study results or may lead to increased risk to the subject in the judgment of the Sub-Investigator. 7_Individuals who use prescription medication or OTC topical medication at the biopsy site(s). 8_Individuals with needle phobia. 9_Individuals with self-reported problems in wound healing and/or disposition to develop extensive scars (keloids, hypertrophic wounds). 10_Individuals who are not prepared to give written informed consent 11_Individuals receiving medical treatment that, in the opinion of the Sub-Investigator, may interfere with this study. 12_Individuals taking medications, that in the opinion of the Sub-Investigator could interfere with this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Collection of skin samples with or without acne vulgaris. Evaluation of the content of sebum secretion and collection of sebum and skin flora.
Secondary Outcome Measures
NameTimeMethod
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