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Efficacy Testing of Hibiscus Sabdariffa Extract and Collagen Products

T

TCI

Status

Completed

Conditions

Skin Condition

Treatments

Dietary Supplement: Hibiscus sabdariffa extract and collagen products
Dietary Supplement: Placebo sachet

Study type

Interventional

Funder types

Industry

Identifiers

NCT05988554
23-048-B

Details and patient eligibility

About

To assess Hibiscus sabdariffa extract and collagen products on skin condition improvement

Enrollment

50 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

50 participants in 2 patient groups, including a placebo group

Placebo sachet
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo sachet
Hibiscus sabdariffa extract and collagen products
Experimental group
Treatment:
Dietary Supplement: Hibiscus sabdariffa extract and collagen products

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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