TCI999 in the Efficacy Verification Program of Hair and Body Health Care
NCT ID: NCT05077553
Last Updated: 2022-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2021-08-17
2022-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
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Placebo sachet
Placebo sachet
Blank
TCI999 probiotic sachet
TCI999 probiotic sachet
Testing product
Interventions
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TCI999 probiotic sachet
Testing product
Placebo sachet
Blank
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with diseases of the skin, liver, kidney.
* Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
* Female who is pregnant or nursing or planning to become pregnant during the course of the study.
* The students taught by the PI.
* Subjects who have wounds on the scalp and subjects who have used drugs to treat the scalp, received hair transplants or other scalp treatments within six months
20 Years
ALL
Yes
Sponsors
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TCI Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Chia-Hua Liang
Role: PRINCIPAL_INVESTIGATOR
Chia Nan University of Pharmacy ＆ Science
Locations
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Chia Nan University of Pharmacy ＆ Science
Tainan City, , Taiwan
Countries
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Other Identifiers
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21-041-A
Identifier Type: -
Identifier Source: org_study_id
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