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A study on the effects of Lactobacillus brevis SBC8803 intake on skin in adults

A study on the effects of Lactobacillus brevis SBC8803 intake on skin in adults - A study on the effects of Lactobacillus brevis SBC8803 intake on skin

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014327
Enrollment
120
Registered
2014-06-20
Start date
2014-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Dry skin

Interventions

Ingestion of placebo capsules for 12 consecutive weeks Ingestion of capsules include Lactobacillus brevis SBC8803 50mg per a day for 12 consecutive weeks Ingestion of capsules include Lactobacillus br

Sponsors

Total Technological Consultant Co., Ltd.(TTC)
Lead Sponsor
SAPPORO BREWERIES LTD.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Males and females between the ages of 20 and 59 2. Higher level of transepidermal water loss on arm

Exclusion criteria

Exclusion criteria: 1. Subjects who have had lactobacillus-rich food, dietary supplements, or medicines constantly 2. Subjects who have used dietary supplements , medicines wchich affects skin constantly 3. Subjects who have treated cosmetic care 4. Subjects who treated cosmetic care except for measuring site or hormonal therapy 5. Subjects who got a facial, a wash-rag, lost hair, or plan these actions 6. Subjects who takes a medicine constantly 7. Subjects who plan to get a tan 8. Subjects who wash the body which provides strong skin irritation 9. Subjects who have a wound or a inflammatory disease 10. Subjects who diagnosed atopy or skin disorders 11. Subjects who have asthma or the possibility of asthma 12. Subjects who have a possibility of having hay fever and gettig a medicine, or is expecdted to develop a symptom of allergic states at the skin in the current study term 13. Subjects who feels to trouble by rough skin around a menstruates 14. Subjects who is employed on a pre-dawn shift or on night duty 15. Subjects who have diabetes, liver disease, kidney disease, or diseases wchich affects a secretion of sex hormones 16. Subjects who have participated in other clinical study 17. Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination 18. Subjects who plans to become pregnant or lactate 19. Subjects who plans to go overseas 20. Subjects who have taken a blood sample or donated blood beyond the limit rules within the last one year prior to the screening test 21. Subjects who take measures affecting the results in current study, or don't stick to the rules 22. Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire 23. Subjects who are judged as unsuitable for the study by physician for other reason

Design outcomes

Primary

MeasureTime frame
Transepidermal water loss

Secondary

MeasureTime frame
Moisture content of the stratum corneum, skin conditions, questionnaire(skin, feces), Athens insomnia scale, Pittsburgh sleep quality index(Japanese)

Countries

Japan

Contacts

Public ContactNAKAGAWA Takashi

Total Technological Consultant Co., Ltd.(TTC) Clinical Research Planning Dept.

t.nakagawa@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026