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A clinical research on the bacterial count measurement for the resident bacterial flora of human skin

A clinical research on the bacterial count measurement for the resident bacterial flora of human skin - A clinical research on the bacterial count measurement for the resident bacterial flora of human skin

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006035
Enrollment
5
Registered
2011-07-25
Start date
2011-07-01
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

Healthy adults

Interventions

The bacillus sample is gathered from the inguinal region on the bacillus sample collection day.

Sponsors

Bio-Iatoric Center, Research Center for Clinical Pharmacology Kitasato University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Not younger than 20 on the day of informed consent (2)Be able to provide written informed consent (3)With healthy dermatological condition, as follows, at the test site -No dermatopathy, such as eczema, dermatitis, or abnormal pigmentation -No wounds or scars -No inflammation due to sunburn -No history of hypersensitivity to drugs -No abnormalities at the test site

Exclusion criteria

Exclusion criteria: (1)With a medical history of skin allergies such as contact dermatitis and atopic dermatitis (2)Received the investigational drug, unapproved drugs, or any treatment using unapproved medical device within 16 weeks prior to informed consent (3)Bathed in swimming pool or public bath within 2 weeks prior to informed consent (4)Bathed in hot tub or took a shower on the day before the bacterial sample collection (5)Received antibacterial drugs, antibiotics, steroids, or other medicine including OTC drugs that might affect the resident bacterial flora of normal skin within 1 week prior to the bacterial sample collection day. (6)Being pregnant, lactating, or at a risk of pregnancy (7)Not willing to contraception (8)Deemed ineligible for participation in the study in the investigator's or the co-investigator's opinion In the criteria of (2), (3) and (5)the day of informed consent or the day of bacterial sample collection is not included in the specified period.

Design outcomes

Primary

MeasureTime frame
Bacterial count in the bacterial sample

Countries

Japan

Contacts

Public ContactTomoko Hasunuma

Bio-Iatoric Center, Research Center for Clinical Pharmacology Bio-Iatoric Center

03-5791-6350

Outcome results

None listed

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