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Efficacy Testing of Collagen and Zhuyin Drinks

T

TCI

Status

Completed

Conditions

Skin Condition

Treatments

Dietary Supplement: Placebo drink
Dietary Supplement: Collagen Cubilose Drink

Study type

Interventional

Funder types

Industry

Identifiers

NCT04266405
20-003-B

Details and patient eligibility

About

To assess collagen and zhuyin drink on skin & body condition improvement

Enrollment

50 patients

Sex

All

Ages

20 to 65 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, 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.
  • Vegetarian
  • Subjects who have large spots (area >3 square centimeter) or abnormal acne.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups, including a placebo group

Placebo drink
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo drink
Collagen and Zhuyin Drinks
Experimental group
Treatment:
Dietary Supplement: Collagen Cubilose Drink

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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