Acne Vulgaris Clinical Trial
Official title:
Studie Van de Huidmicrobiota en Het Potentieel Van Een crème Met Probiotica Bij Personen Met Acne
Verified date | March 2018 |
Source | University Hospital, Antwerp |
Contact | Julien Lambert, Prof. dr. |
Phone | 038213223 |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this study the topical use of cream with live probiotic bacteria was evaluated for its efficacy in reducing acne symptoms and its effect on the skin microbiota on patients with acne. Patients with mild to moderate acne used the probiotic cream for 8 weeks and clinical evaluation and sampling was done at start, 4, 8 and 10 weeks. Next-Generation Sequencing was used to analyze the skin microbiota of the patients.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | March 31, 2018 |
Est. primary completion date | December 14, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 12 Years to 25 Years |
Eligibility |
Inclusion Criteria: - mild to moderate acne Exclusion Criteria: - local treatments, including cleansers, soaps, antimycotics and antibiotics within 2 weeks prior to start of study - use of oral antibiotics within 4 weeks prior to start of study - use of systemic retinoids within 6 months prior to start of study |
Country | Name | City | State |
---|---|---|---|
Belgium | University Hospital, Antwerp | Edegem | Antwerp |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Antwerp |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Skin microbiome differences | Analysis of the skin's microbiome at start (baseline) and after treatment with the ACN Cream | baseline; after 4 and 8 weeks of treatment; at 10 weeks, i.e. 2 weeks after stop of treatment | |
Primary | Clinical acne symptoms | Clinical evaluation of acne symptoms | baseline, at 4, 8 and 10 weeks |
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