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Completed

NCT Number: NCT05143034

the Evaluation of the Efficacy of TCI66207 on the Skin.

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

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Key information

Conditions

Skin Diseases Skin and Connective Tissue Diseases

Age range

20 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Research & Design Center, TCI CO., Ltd

Taipei, Neipu Township, 114, Taiwan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • .Subject with diseases of the skin, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history).
  • 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.
  • Received facial laser therapy, chemical peeling or UV overexposure in the past 4 weeks.
  • Subjects who have large spots (area >3 square centimeter) or abnormal acne.

Treatment and study plan

TCI66207 Essence

Dietary Supplement

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

Placebo Essence

Dietary Supplement

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

Primary outcomes

  1. The change of skin moisture

    Time frame: Subjects will be tested in the 4th week.

    Corneometer® CM825 was utilized to measure skin moisture. Units: arbitrary Corneometer® units 0-120

  2. The change of skin elasticity

    Time frame: Subjects will be tested in the 4th week.

    Cutometer® dual MPA 580 was utilized to measure skin elasticity (parameter R2). Units: μm penetration depth into the probe opening, expressed as curvesCorneometer® units 0-120

  3. The change of skin wrinkles

    Time frame: Subjects will be tested in the 4th week.

    VISIA Complexion Analysis System was utilized to measure wrinkles. Units: arbitrary units

  4. The change of skin collagen density

    Time frame: Subjects will be tested in the 4th week.

    DermaLab® USB - 20 MHz High Freq. Ultrasound probe was utilized to scan and analyze skin collagen density. Units: Intensity score

  5. The change of skin texture

    Time frame: Subjects will be tested in the 4th week.

    VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units

  6. The change of skin pores

    Time frame: Subjects will be tested in the 4th week.

    VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units

Sponsors and collaborators

Lead sponsor

TCI Co., Ltd.

Industry

Registry information

Official study title

Evaluation of Skin Efficacy of TCI66207

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Dec 3, 2021
Registry last updated
Dec 7, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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