TCI999 in the Efficacy Verification Program of Hair and Body Health Care

TCI

Status: Completed

Conditions: Hair Loss

Treatments: Dietary Supplement: TCI999 probiotic sachet; Dietary Supplement: Placebo sachet

Study type: Interventional

Funder types: Industry

Identifiers

NCT05077553

21-041-A

Details and patient eligibility

About

To assess TCI999 on hair and body health care

Enrollment: 50 patients

Sex: All

Ages: 20+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy adults aged above 20 years old

Exclusion criteria

• Subject who is not willing to participate in this study.
• 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

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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50 participants in 2 patient groups, including a placebo group

Placebo sachet

Placebo Comparator group

Treatment:

Dietary Supplement: Placebo sachet

TCI999 probiotic sachet

Experimental group

Treatment:

Dietary Supplement: TCI999 probiotic sachet