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Efficacy Evaluation of TCI153 Probiotics for Skin Beautification

T

TCI

Status

Completed

Conditions

Skin Condition

Treatments

Dietary Supplement: TCI153 probiotic sachet
Dietary Supplement: Placebo sachet

Study type

Interventional

Funder types

Industry

Identifiers

NCT06166342
23-091-B

Details and patient eligibility

About

To assess TCI153 prebiotics product on skin condition improvement

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults aged above 18 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.
  • Received facial laser therapy, chemical peeling or UV overexposure (> 3 hr/week) in the past 4 weeks.
  • Constant drug use
  • Students who are currently taking courses taught by the principal investigator of this trial.
  • Subject who is not willing to have their photos published in public.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups, including a placebo group

Placebo sachet
Placebo Comparator group
Description:
consume 1 sachet per day
Treatment:
Dietary Supplement: Placebo sachet
TCI153 sachet
Experimental group
Description:
consume 1 sachet per day
Treatment:
Dietary Supplement: TCI153 probiotic sachet

Trial contacts and locations

1

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Central trial contact

Chia-Hua Liang; Ping Lin

Data sourced from clinicaltrials.gov

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