the Evaluation of the Efficacy of TCI66207 on the Skin.

NCT ID: NCT05143034

Last Updated: 2021-12-07

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-11-01

Study Completion Date

2019-12-31

Brief Summary

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The purpose of this study is to explore the evaluation of the efficacy of TCI66207 deep-sea live-face bacteria on the skin.

Detailed Description

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Conditions

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Skin Diseases

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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TCI66207 Essence

Essence

Group Type EXPERIMENTAL

TCI66207 Essence

Intervention Type DIETARY_SUPPLEMENT

Use it twice a day after washing your face in the morning and evening for a total of 4 weeks.

Placebo Essence

Group Type PLACEBO_COMPARATOR

Placebo Essence

Intervention Type DIETARY_SUPPLEMENT

Use it twice a day after washing your face in the morning and evening for a total of 4 weeks.

Interventions

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TCI66207 Essence

Use it twice a day after washing your face in the morning and evening for a total of 4 weeks.

Intervention Type DIETARY_SUPPLEMENT

Placebo Essence

Use it twice a day after washing your face in the morning and evening for a total of 4 weeks.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

1. Healthy volunteers aged above 20 years old
2. Subject has dull skin.

Exclusion Criteria

1. .Subject with diseases of the skin, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history).
2. Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
3. Female who is pregnant or nursing or planning to become pregnant during the course of the study.
4. Received facial laser therapy, chemical peeling or UV overexposure in the past 4 weeks.
5. Subjects who have large spots (area \>3 square centimeter) or abnormal acne.
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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TCI Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chia-Hua Liang, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Chia Nan University of Pharmacy & Science

Locations

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Research & Design Center, TCI CO., Ltd

Taipei, Neipu Township, Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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TSMH No.18-148-A

Identifier Type: -

Identifier Source: org_study_id