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Efficacy Testing of Chenopodium Formosanum Extracts on Skin Beauty

T

TCI

Status

Completed

Conditions

Skin Condition

Treatments

Dietary Supplement: Placebo sachet
Dietary Supplement: Chenopodium formosanum extracts sachet

Study type

Interventional

Funder types

Industry

Identifiers

NCT05591352
22-043-B

Details and patient eligibility

About

To assess Chenopodium formosanum extracts on skin condition improvement

Enrollment

300 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.
  • 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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

300 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
Chenopodium formosanum extracts sachet
Experimental group
Description:
consume 1 sachet per day
Treatment:
Dietary Supplement: Chenopodium formosanum extracts 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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