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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03469076
Other study ID # 16/14/168
Secondary ID B300201628507
Status Recruiting
Phase N/A
First received March 12, 2018
Last updated March 12, 2018
Start date April 25, 2016
Est. completion date March 31, 2018

Study information

Verified date March 2018
Source University Hospital, Antwerp
Contact Julien Lambert, Prof. dr.
Phone 038213223
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Probiotics are live micro-organisms which when administered in adequate amounts can exert a health benefit on the host. This health-promoting effects have been extensively studied in the gastrointestinal niche but it becomes more and more clear that other niches are also interesting for the potential of probiotics. Recent breakthroughs in 'next generation sequencing' (NGS) technologies are making it now possible to map the microbiota after DNA extraction, which is very interesting for bacteria that are not or difficult to cultivate. The research into the microbiota of the skin with such new NGS technologies currently limited, but shows that there is also an equilibrium in the skin composition of the microbiota and that there is a disturbance of the skin microbiota in acne (Murillo & Raoult, 2013). In acne vulgaris it is known that the condition is multifactorial and that both hormonal triggers and environmental factors play a role. However, it is also known that Propionibacterium acnes play an important role in the inflammation of the sebaceous gland follicles. Probiotic strains with antipathogenic activity against this bacterium and suitable for application to the skin is thus potentially able to restore the balance of the skin microbiota and reduce acne symptoms.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
YUN ACN Cream
YUN ACN Cream with live probiotic bacteria (min. 10-6 à 10-7 CFU per application) applied twice daily (morning and evening) on the entire face

Locations

Country Name City State
Belgium University Hospital, Antwerp Edegem Antwerp

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Antwerp

Country where clinical trial is conducted

Belgium, 

Outcome

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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