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Efficacy Testing of Crassocephalum Rabens Extract Capsules

G

Greenyn Biotechnology

Status

Completed

Conditions

Aging

Treatments

Dietary Supplement: Crassocephalum rabens extract

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT05309161
21-129-A

Details and patient eligibility

About

This study is to investigate the improveing effects of the Crassocephalum rebens extract on skin conditions in normal people.

Enrollment

40 patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age over 20 years
  2. Healthy people

Exclusion criteria

  1. Non-volunteer
  2. Pregnant and lactating women
  3. Hypersensitivity to the assigned product
  4. Diagnosed with skin diseases, liver diseases, kinedy disease, and other severe diseases
  5. Cosmetic, drug, or food allergies
  6. Concurrent aesthetic treatments (e.g., intense pulse light, medical peelings, or laser therapy)
  7. Aceepted aesthetic treatments one month ago before the study
  8. Chronic sun exposure (over 3 hours/day)
  9. The members of the research team

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups, including a placebo group

A group (placebo)
Placebo Comparator group
Description:
Placebo
Treatment:
Dietary Supplement: Crassocephalum rabens extract
B group (experimental)
Active Comparator group
Description:
Crassocephalum rabens extract
Treatment:
Dietary Supplement: Crassocephalum rabens extract

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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