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clinical efficacy and mechanism of Bifidobacterium lactis M8 in patients with facial acne

clinical efficacy and mechanism of Bifidobacterium lactis M8 in patients with facial acne

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017745
Enrollment
Unknown
Registered
2018-08-12
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

facial acne

Interventions

test group:bifidobacterium lactis m8
control group:placebo

Sponsors

Weihai Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Meet the diagnostic criteria for acne; Gender unlimited; Aged 18~25 years old; Able to complete the questionnaire survey; Voluntarily participate in this study and sign informed consent, during treatment, no food and beverage with spicy, thick flavor and probiotics is allowed.

Exclusion criteria

Exclusion criteria: Oral antibiotics, glucocorticoids, immunosuppressants and other drugs in the past 1 month, Using external drugs for the face; Pregnant and lactating women; Complicated with gastrointestinal diseases or gastrointestinal history of surgery, hypertension, diabetes, heart, liver, kidney dysfunction and other systemic diseases.

Design outcomes

Primary

MeasureTime frame
skin lesion type;number of lesions;number of intestinal flora;blood lipid;blood lipid;testosterone;

Countries

China

Contacts

Public ContactYu Xuehong

Weihai Municipal Hospital

18660377339@163.com+86 18660377339

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026